Membrane partition system for plating of wafers

Information

  • Patent Grant
  • 6569299
  • Patent Number
    6,569,299
  • Date Filed
    Thursday, May 18, 2000
    24 years ago
  • Date Issued
    Tuesday, May 27, 2003
    21 years ago
Abstract
An anode includes an anode cup, a membrane and ion source material, the anode cup and membrane forming an enclosure in which the ion source material is located. The anode cup includes a base section having a central aperture and the membrane also has a central aperture. A jet is passed through the central apertures of the base section of the anode cup and through the membrane allowing plating solution to be directed at the center of a wafer being electroplated.
Description




FIELD OF INTENTION




The present invention relates generally to electroplating and more particularly an anode for an electroplating system.




BACKGROUND OF THE INVENTION




The manufacture of semiconductor devices often requires the formation of electrical conductors on semiconductor wafers. For example, electrically conductive leads on the wafer are often formed by electroplating (depositing) an electrically conductive material such as copper on the wafer and into patterned trenches.




Electroplating involves making electrical contact with the wafer surface upon which the electrically conductive layer is to be deposited (hereinafter the “wafer plating surface”). Current is then passed through a plating solution (i.e. a solution containing ions of the element being deposited, for example a solution containing Cu


++


) between an anode and the wafer plating surface (the wafer plating surface being the cathode). This causes an electrochemical reaction on the wafer plating surface which results in the deposition of the electrically conductive layer.




Generally, electroplating systems use soluble or insoluble anodes. Insoluble anodes tend to evolve oxygen bubbles which adhere to the wafer plating surface. These oxygen bubbles disrupt the flow of ions and electrical current to the wafer plating surface creating nonuniformity in the deposited electrically conductive layer. For this reason, soluble anodes are frequently used.




Soluble anodes are not without disadvantages. One disadvantage is that soluble anodes, by definition, dissolve. As a soluble anode dissolves, it releases particulates into the plating solution. These particulates can contaminate the wafer plating surface, reducing the reliability and yield of the semiconductor devices formed on the wafer.




One conventional technique of reducing particulate contamination is to contain the soluble anode in a porous anode bag. However, while preventing large size particulates and chunks from being released into the plating solution, conventional anode bags fail to prevent smaller sized particulates from entering the plating solution and contaminating the wafer plating surface.




Another conventional technique of reducing particulate contamination is to place a filter between the anode and the article to be electroplated as set forth in Reed, U.S. Pat. No. 4,828,654 (hereinafter Reed). Referring to FIG. 2 of Reed, filters 60 are positioned between anode arrays 20 and a printed circuit board 50 (PCB 50). Filters 60 allows only ionic material of a relatively small size, for example one micron, to pass from anode arrays 20 to PCB 50. While allowing relatively small size particulates to pass through, filters 60 trap larger sized particulates avoiding contamination of PCB 50 from these larger sized particulates. Over time, however, filters 60 become clogged by these larger sized particulates.




To reduce clogging of filters 60, Reed provides a counterflow of plating solution through filters 60 in a direction from PCB 50 towards anode arrays 20. This counterflow tends to wash some of the larger sized particulates from filters 60. However, even with the counterflow, eventually filters 60 become clogged. To allow servicing of filters 60, retaining strips 66 and support strips 68 allow filters 60 to be removed and cleaned when filters 60 eventually become clogged.




Although providing a convenient means of cleaning filters 60, removal of filters 60 necessarily releases the larger sized particulates from within the vicinity of anode arrays 20 into the entire system and, in particular, into the vicinity where PCBs 50 are electroplated. Even after filters 60 are cleaned and replaced, this contamination of the system can cause contamination of a subsequently electroplated PCB 50 reducing the reliability and yield of the printed circuit boards. Further, even with filters 60, particulates accumulate on receptacle 14 in the vicinity of anode arrays 20 and the system must periodically be shut down and drained of plating solution to clean these particulates from receptacle 14.




In addition to creating particulates, a soluble anode changes shape as it dissolves, resulting in variations in the electric field between the soluble anode and the wafer. Of importance, the thickness of the electrically conductive layer deposited on the wafer plating surface depends upon the electric field. Thus, variations in the shape of the soluble anode result in variations in the thickness of the deposited electrically conductive layer across the wafer plating surface. However, it is desirable that the electrically conductive layer be deposited uniformly (have a uniform thickness) across the wafer plating surface to minimize variations in characteristics of devices formed on the wafer.




Another disadvantage of soluble anodes is passivation. As is well known to those skilled in the art, the mechanism by which anode passivation occurs depends upon a variety of factors including the process conditions, plating solution and anode material. Generally, anode passivation inhibits dissolution of the anode while simultaneously preventing electrical current from being passed through the anode and should be avoided.




SUMMARY OF THE INVENTION




In accordance with the present invention an anode includes an anode cup, a membrane and ion source material. The anode source material is located in an enclosure formed by the anode cup and membrane. The anode cup and membrane both have central apertures through which a jet (a tube) is passed. During use, plating solution flows through the jet.




By passing the jet through the center of the anode, plating solution from the jet is directed at the center of the wafer being electroplated. This enhances removal of gas bubbles entrapped on the wafer plating surface and improves the uniformity of the deposited electrically conductive layer on the wafer.




The membrane has a porosity sufficient to allow ions from the ion source material, and hence electrical current, to flow through the membrane. Although allowing electrical current to pass, the membrane has a high electrical resistance which produces a voltage drop across the membrane during use. This high electrical resistance redistributes localized high electrical currents over larger areas improving the uniformity of the electric current flux to the wafer which, in turn, improves the uniformity of the deposited electrically conductive layer on the wafer.




In addition to having a porosity sufficient to allow electrical current to pass, the membrane also has a porosity sufficient to allow plating solution to flow through the membrane. However, to prevent particulates generated by the ion source material from passing through the membrane and contaminating the wafer, the porosity of the membrane prevents contaminant particulates from passing through the membrane.




Of importance, when the membrane becomes clogged with particulates, the anode can be readily removed from the electroplating system. After removal of the anode, the membrane can be separated from the anode cup and cleaned or replaced. Advantageously, cleaning of the membrane is accomplished outside of the plating bath and, accordingly, without releasing particulates from inside of the anode into the plating bath.




In one embodiment, the jet includes a plating solution inlet through which plating solution flows from the jet into the enclosure formed by the anode cup and membrane and across the ion source material. The flow of plating solution across the ion source material prevents anode passivation. The plating solution then exits the enclosure via two routes. First, some of the plating solution exits through the membrane. As discussed above, contaminant particulates generated as the ion source material dissolves do not pass through the membrane and accordingly do not contaminate the wafer. Second, some of the plating solution exits through outlets located at the top of a wall section of the anode cup. These outlets are plumbed to an overflow receiver and thus the plating solution which flows through these outlets does not enter the plating bath and does not contaminate the wafer. Further, by locating these outlets at the top of the wall section of the anode cup, gas bubbles entrapped under the membrane are entrained with the exiting plating solution and readily removed from the anode.




These and other objects, features and advantages of the present invention will be more readily apparent from the detailed description of the preferred embodiments set forth below taken in conjunction with the accompanying drawings.











BRIEF DESCRIPTION OF THE DRAWINGS





FIG. 1

is a diagrammatic view of an electroplating apparatus having a wafer mounted therein in accordance with the present invention.





FIG. 2

is a cross-sectional view of an anode in accordance with the present invention.





FIGS. 3 and 4

are cross-sectional views of anodes in accordance with alternative embodiments of the present invention.











DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS




Several elements in the following figures are substantially similar. Therefore similar reference numbers are used to represent similar elements.





FIG. 1

is a diagrammatic view of an electroplating apparatus


30


having a wafer


38


mounted therein in accordance with the present invention. Apparatus


30


includes a clamshell


32


mounted on a rotatable spindle


40


which allows rotation of clamshell


32


. Clamshell


32


comprises a cone


34


, a cup


36


and a flange


48


. Flange


48


has formed therein a plurality of apertures


50


. A clamshell lacking a flange


48


yet in other regards similar to clamshell


32


is described in detail in Patton et al., co-filed application Ser. No. 08/969,984, cited above. A clamshell including a flange similar to clamshell


32


is described in detail in Contolini et al., co-filed application Ser. No. 08/970,120, cited above.




During the electroplating process, wafer


38


is mounted in cup


36


. Clamshell


32


and hence wafer


38


are then placed in a plating bath


42


containing a plating solution. As indicated by arrow


46


, the plating solution is continually provided to plating bath


42


by a pump


44


. Generally, the plating solution flows upwards to the center of wafer


38


and then radially outward and across wafer


38


through apertures


50


as indicated by arrows


52


. Of importance, by directing the plating solution towards the center of wafer


38


, any gas bubbles entrapped on wafer


38


are quickly removed through apertures


50


. Gas bubble removal is further enhanced by rotating clamshell


32


and hence wafer


38


.




The plating solution then overflows plating bath


42


to an overflow reservoir


56


as indicated by arrows


54


. The plating solution is then filtered (not shown) and returned to pump


44


as indicated by arrow


58


completing the recirculation of the plating solution.




A DC power supply


60


has a negative output lead


210


electrically connected to wafer


38


through one or more slip rings, brushes and contacts (not shown). The positive output lead


212


of power supply


60


is electrically connected to an anode


62


located in plating bath


42


. During use, power supply


60


biases wafer


38


to have a negative potential relative to anode


62


causing an electrical current to flow from anode


62


to wafer


38


. (As used herein, electrical current flows in the same direction as the net positive ion flux and opposite the net electron flux.) This causes an electrochemical reaction (e.g. Cu


++


+2e





=Cu) on wafer


38


which results in the deposition of the electrically conductive layer (e.g. copper) on wafer


38


. The ion concentration of the plating solution is replenished during the plating cycle by dissolving anode


62


which comprises, for example, a metallic compound (e.g. Cu=Cu


++


+2e





) as described in detail below. Shields


53


and


55


(virtual anodes) are provided to shape the electric field between anode


62


and wafer


38


. The use and construction of shields are further described in Reid et al., co-filed application Ser. No. 08/969,267, cited above.




As shown in

FIG. 1

, the plating solution is provided to plating bath


42


and directed at wafer


38


by a jet of plating solution indicated by arrow


46


. Referring now to

FIG. 2

, a cross-sectional view of anode


62


A having a jet


200


passing through the center is illustrated. Jet


200


typically consists of a tube formed of an electrically insulating material. Anode


62


A comprises an anode cup


202


, contact


204


, ion source material


206


, and a membrane


208


.




Anode cup


202


is typically an electrically insulating material such as polyvinyl chloride (PVC), polypropylene or polyvinylidene flouride (PVDF). Anode cup


202


comprises a disk shaped base section


216


having a central aperture


214


through which jet


200


passes. An O-ring


310


forms the seal between jet


200


and base section


216


of anode cup


202


. Anode cup


202


further comprises a cylindrical wall section


218


integrally attached at one end (the bottom) to base section


216


.




Contact


204


is typically an electrically conductive relatively inert material such as titanium. Further, contact


204


can be fashioned in a variety of forms, e.g. can be a plate with raised perforations or, as illustrated in

FIG. 2

, a mesh. Contact


204


rests on base section


216


of anode cup


202


. Positive output lead


212


from power supply


60


(see

FIG. 1

) is formed of an electrically conductive relatively inert material such as titanium. Lead


212


is attached, typically bolted, to a rod


270


which is also formed of an electrically conductive relatively inert material such as titanium. Rod


270


passes through anode cup


202


to make the electrical connection with contact


204


.




Resting on and electrically connected with contact


204


is ion source material


206


, for example copper. Ion source material


206


comprises a plurality of granules. These granules can be fashioned in a variety of shapes such as in a spherical, nugget, flake or pelletized shape. In one embodiment, copper balls having a diameter in the range of 1.0 centimeters to 2.54 centimeters are used. Alternatively, ion source material


206


comprises an single integral piece such as a solid disk of material. During use, ion source material


206


electrochemically dissolves (e.g. Cu=Cu


2+


+2e





) replenishing the ion concentration of the plating solution.




Ion source material


206


is contained in an enclosure formed by anode cup


202


, membrane


208


and jet


200


. More particularly, membrane


208


is attached, typically welded, to a seal ring


312


at a central aperture


207


of membrane


208


and to a seal ring


314


at its outer circumference. Seal rings


312


,


314


are formed of materials similar to those discussed above for anode cup


202


. Seal ring


312


forms a seal with jet


200


by an O-ring


316


and seal ring


314


forms a seal with a second end (the top) of wall section


218


of anode cup


202


by an O-ring


318


. By attaching membrane


208


to seal rings


312


,


314


, membrane


208


forms a seal at its outer circumference with the top of wall section


218


of anode cup


202


and also forms a seal with jet


200


at central aperture


207


of membrane


208


. Suitable examples of membrane


208


include: napped polypropylene available from Anode Products, Inc. located in Illinois; spunbond snowpro polypropylene and various polyethylene, RYTON, and TEFLON materials in felt, monofilament, filament and spun forms available from various suppliers including Snow Filtration, 6386 Gano Rd., West Chester, Ohio.




In an alternative embodiment, membrane


208


is itself formed of a material having a sufficient rigidity to form a pressure fit with wall section


218


and jet


200


and seal rings


312


,


314


are not provided.




Membrane


208


has a porosity sufficient to allow ions from ion source material


206


, and hence electrical current, to flow through membrane


208


. Although allowing electrical current to flow through, membrane


208


has a high electrical resistance which produces a voltage drop across membrane


208


from lower surface


209


to upper surface


211


. This advantageously minimizes variations in the electric field from ion source material


206


as it dissolves and changes shape.




As an illustration, absent membrane


208


, a region of ion source material


206


having a high electrical conductivity relative to the remainder of ion source material


206


would support a relatively high electrical current. This in turn would provide a relatively high electric current flux to the portion of the wafer directly above this region of ion source material


206


, resulting in a greater thickness of the deposited electrically conductive layer on this portion of the wafer. However, by providing electrically resistive membrane


208


, the relatively high electrical current from this region of ion source material


206


redistributes over a larger area to find the path of least resistance through membrane


208


. Redistributing the relatively high electrical current over a larger area improves the uniformity of the electric current flux to the wafer which, in turn, improves the uniformity of the deposited electrically conductive layer.




In addition to having a porosity sufficient to allow electrical current to flow through, membrane


208


also has a porosity sufficient to allow plating solution to flow through membrane


208


, i.e. has a porosity sufficient to allow liquid to pass through membrane


208


. However, to prevent particulates generated by ion source material


206


from passing through membrane


208


and contaminating the wafer, the porosity of membrane


208


prevents large size particulates from passing through membrane


208


. Generally, it is desirable to prevent particulates greater in size than one micron (1.0 μm) from passing through membrane


208


and in one embodiment particulates greater in size than 0.1 μm are prevented from passing through membrane


208


.




Of importance, when membrane


208


becomes clogged with particulates such that electric current and plating solution flow through membrane


208


is unacceptably inhibited, anode


62


A can readily be removed from plating bath


42


A. After removal of anode


62


A, membrane


208


is separated from anode cup


202


and cleaned or replaced. Advantageously, cleaning of membrane


208


is accomplished outside of plating bath


42


A and, accordingly, without releasing particulates from inside of anode


62


A into plating bath


42


A. This is in contrast to Reed (cite above) wherein cleaning of the membrane necessarily releases particulates into the bulk of the plating solution. In further contrast to Reed, use of anode


62


A including anode cup


202


and membrane


208


prevents particulate accumulation anywhere on plating bath


42


A.




To prevent anode passivation, plating solution is directed into the enclosure formed by anode cup


202


and membrane


208


and across ion source material


206


. As those skilled in the art understand, a flow of plating solution across an anode prevents anode passivation. The flow of plating solution into anode cup


202


is provided at several locations.




In this embodiment, jet


200


is fitted with a plating solution inlet


220


located between membrane


208


and base section


216


. A portion of the plating solution flowing through jet


200


is diverted through inlet


220


and into anode cup


202


. To prevent inadvertent backflow of plating solution and particulates from anode cup


202


into jet


200


, inlet


220


is fitted with a check valve which allows the plating solution only to flow from jet


200


to anode cup


202


and not vice versa.




Jet


200


is also provided with a plating solution outlet


224


which is connected by a tube


230


to an inlet


228


on base section


216


of anode cup


202


. In this manner, a portion of the plating solution from jet


200


is directed into the bottom of anode cup


202


. Outlet


224


is fitted with a check valve to prevent backflow of plating solution and particulates from anode cup


202


into jet


200


.




Jet


200


is also provided with an outlet


232


connected by a tube


234


to an inlet


236


on wall section


218


of anode cup


202


. In this manner, a portion of the plating solution from jet


200


is directed into the side of anode cup


202


. Outlet


232


is fitted with a check valve to prevent backflow of plating solution and particulates from anode cup


202


into jet


200


.




Although inlets


228


,


236


on anode cup


202


are connected to outlets


224


,


232


on jet


200


, respectively, in other embodiments (not shown), inlets


228


,


236


are connected to an alternative source of plating solution. For example, inlets


228


,


236


are connected to a pump which pumps plating solution to inlets


228


,


236


through tubing. Further, although plating solution is provided to anode cup


202


from inlets


220


,


228


,


236


, in other embodiments (not shown), only one or more of inlets


220


,


228


and


236


are provided. For example, solution flow is directed into anode cup


202


through inlet


220


only and inlets


228


,


236


(and corresponding outlets


224


,


232


, check valves and tubes


230


,


234


, respectively) are not provided. Alternatively, a plurality of inlets


220


,


228


,


236


can be provided.




Referring still to

FIG. 2

, the plating solution introduced into anode cup


202


then flows out of anode cup


202


via two routes. First, some of the plating solution flows through membrane


208


and into plating bath


42


A. As discussed above, the porosity of membrane


208


allows plating solution to pass through yet prevents particulates over a certain size from passing through (hereinafter referred to as contaminant particulates). Thus, contaminant particulates generated as ion source material


206


dissolves do not pass through membrane


208


and into plating bath


42


A and accordingly do not contaminate the wafer being electroplated. This is in contrast to conventional anode bags which allow unacceptably large (e.g. greater than 1.0 μm) particulates to pass through.




In addition to flowing through membrane


208


, plating solution exits through outlets


240


,


242


of anode cup


202


. From outlets


240


,


242


, the plating solution flows through tubes


244


,


246


, though outlets


248


,


250


of plating bath


42


A and into overflow reservoir


56


A. Check valves (not shown) can be provided to prevent backflow of plating solution from overflow reservoir


56


A to anode cup


202


. From overflow reservoir


56


A, the plating solution is filtered to remove particulates including contaminant particulates and then returned to plating bath


42


A and jet


200


.




Of importance, plating solution removed from anode cup


202


through outlets


240


,


242


does not directly enter plating bath


42


A without first being filtered to remove contaminant particulates. Thus, outlets


240


,


242


support a sufficient flow of plating solution through anode cup


202


to prevent anode passivation to the extent that membrane


208


does not.




Further, by locating outlets


240


,


242


at the second end (top) of wall section


218


of anode cup


202


, gas bubbles entrapped inside of anode cup


202


, and more particularly, gas bubbles entrapped under membrane


208


are readily removed to overflow reservoir


56


A.




Gas bubble removal is further enhanced by shaping membrane


208


as a frustum of an inverted right circular cone having a base at wall section


218


and an apex at jet


200


. More particularly, by having the distance A between membrane


208


and base section


216


at wall section


218


greater than the distance B between membrane


208


and base section


216


at jet


200


, gas bubbles entrapped under membrane


208


tend to move across membrane


208


from jet


200


to wall section


218


. At wall section


218


, these gas bubbles become entrained with the plating solution flowing through outlets


240


,


242


and are removed into overflow reservoir


56


A. Advantageously, these gas bubbles do not enter plating bath


42


A and travel to the wafer and accordingly do not create nonuniformity in the deposited electrically conductive layer on the wafer.





FIG. 3

is a cross-sectional view of an anode


62


B and jet


200


B in accordance with an alternative embodiment of the present invention. In this embodiment, anode cup


202


B has a perforated base section


216


B comprising a plurality of apertures


256


extending from a lower surface


219


to an upper surface


221


of perforated base section


216


B. Anode


62


B further comprises a filter sheet


258


on upper surface


221


of perforated base section


216


B. Contact


204


B rests on filter sheet


258


and thereby on perforated base section


216


B. Filter sheet


258


readily allows plating solution to flow through yet prevents contaminant particulates from passing through.




During use, plating solution is provided to jet


200


B. Plating solution is also provided to plating bath


42


B such that the plating solution flows upwards in plating bath


42


B towards perforated base section


216


B. As the plating solution encounters perforated base section


216


B, a portion of the plating solution is diverted around anode cup


202


B as indicated by arrows


254


. Further, a portion of the plating solution flows through apertures


256


, through filter sheet


258


and into anode cup


202


B. The plating solution then flows across ion source material


206


B preventing anode passivation.




The plating solution then exits anode cup


202


B through membrane


208


B and outlets


240


B,


242


B as described above in reference to anode


62


A (FIG.


2


). In contrast to anode


62


A, anode


62


B (

FIG. 3

) allows plating solution to directly enter anode cup


202


B without the use of any additional tubing, checkvalves and associated inlets/outlets. In addition, there is greater flexibility in setting the flow rate of plating solution through jet


200


B since plating solution is provided to anode cup


202


B independent of jet


200


B.




In anodes


62


A,


62


B of FIGS.


2


,


3


, membranes


208


,


208


B enable jets


200


,


200


B, respectively, to pass through the center of the anode. Advantageously, this allows plating solution from jets


200


,


200


B to be directed at the center of the wafer being electroplated, enhancing removal of gas bubbles entrapped on the wafer plating surface and improving the uniformity of the deposited electrically conductive layer on the wafer. This is in contrast to conventional anode bags which do not allow the possibility of a configuration which passes a jet through the middle of the anode.





FIG. 4

is a cross-sectional view of an anode


62


C and jet


200


C in accordance with an alternative embodiment of the present invention. In this embodiment, jet


200


C does not extend through the center of anode


62


C but extends horizontally from plating bath


42


C and curves upwards to direct plating solution at the center of the wafer (not shown) being electroplated. Accordingly, membrane


208


C is a disk shaped integral membrane, i.e. does not have an aperture through which jet


200


C passes. Anode cup


202


C is provided with a perforated base section


216


C having a plurality of apertures


256


C. To prevent anode passivation, plating solution, enters anode cup


202


C through apertures


256


C of perforated base section


216


C and then exits through membrane


208


C.




At the second end (top) of wall section


218


C of anode cup


202


C, a shield


55


C is located. Shield


55


C is formed of an electrically insulating material and reduces the electric field and electric current flux at the edge region of the wafer plating surface. This reduces the thickness of the deposited electrically conductive layer on this edge region of the wafer plating surface thus compensating for the edge effect. (The edge effect is the tendency of the deposited electrically conductive layer to be thicker at the edge region of the wafer plating surface.) The edge effect is described in detail in Contolini et al., co-filed application Ser. No. 08/970,120 and the use of shields is describe in detail in Reid et al., co-filed application Ser. No. 08/969,267, both cited above. (Referring to

FIG. 2

, seal rings


312


,


314


may also act as shields and reduce the electric field and electric current flux to the center region and edge region, respectively, of the wafer plating surface.)




Illustrative specifications for various characteristics of anode


62


C, jet


200


C and plating bath


42


C shown in

FIG. 4

are provided in Table I below.














TABLE I









CHARACTERISTIC




DESCRIPTION




SPECIFICATION











C




Plating bath




11.000 In. 







Diameter






D




Anode cup




9.000 In.







Diameter






E




Membrane outside




8.000 In.







Diameter






F




Jet opening depth




1.500 In.






G




Jet entry depth




2.000 In.






H




Anode cup depth




3.000 In.






I




Anode cup




1.500 In.







thickness






J




Plating bath




4.890 In.







depth






K




Plating bath




7.051 In.







total height














Having thus described the preferred embodiments, persons skilled in the art will recognize that changes may be made in form and detail without departing from the spirit and scope of the invention. For example, although the membrane is described as highly electrically resistive, the membrane can be highly electrically conductive. Further, the porosity of the membrane depends upon the maximum acceptance size particulates allowable into the plating bath. Thus, the porosity of membrane, depending upon the application, may allow particulates much greater or much less than 1.0 μm in size to pass through. Further, the membrane should allow ions to pass through but may or may not allow plating solution to flow through. Thus the invention is limited only by the following claims.



Claims
  • 1. An electroplating system for semiconductor wafers comprising:a power supply having a negative terminal and a positive terminal; a semiconductor wafer electrically connected to the negative terminal; a plating bath holding a plating solution; an anode positioned in the plating solution and electrically connected to the positive terminal; a pump for creating a flow of plating solution generally in a direction from the anode towards the wafer; and a porous membrane positioned downstream from the anode in the flow of plating solution.
  • 2. The electroplating system of claim 1 wherein the anode comprises a plurality of granules.
  • 3. The electroplating system of claim 1 wherein the anode consists essentially of a single piece of material.
  • 4. The electroplating system of claim 1 wherein the anode is a single piece of material.
  • 5. The electroplating system of claim 3 or 4 wherein the anode is in the shape of a disk.
  • 6. The electroplating system of claim 1 wherein the flow of plating solution is generally upward, the porous membrane being positioned above the anode.
  • 7. The electroplating system of claim 1 wherein the porous membrane is fitted against a wall of the plating bath.
  • 8. The electroplating system of claim 1 wherein the membrane has a porosity sufficient to allow ions from the anode to pass through the membrane.
  • 9. The electroplating system of claim 1 wherein the membrane has a porosity sufficient to allow the plating solution to pass through the membrane.
  • 10. The electroplating system of claim 1 wherein the membrane has a porosity sufficient to prevent particulates from the anode greater than one micron in size to pass through the membrane.
  • 11. The electroplating system of claim 1 wherein the porous membrane is disk shaped.
  • 12. The electroplating system of claim 1 wherein the anode comprises a plurality of apertures through which the plating solution passes.
  • 13. The electroplating system of claim 1 comprising a nonconductive shield positioned downstream from the anode in the flow of plating solution, the shield comprising an annular member with an aperture having a diameter less than a diameter of the anode.
  • 14. The electroplating system of claim 13 wherein the diameter of the aperture of the shield is less than a diameter of the wafer.
CROSS REFERENCE TO RELATED APPLICATION

This application is related to Patton et al., co-filed application Ser. No. 08/969,984, filed Nov. 13, 1997, now U.S. Pat. No. 6,156,167, Reid et al., co-filed application Ser. No. 08/969,267, filed Nov. 13, 1997, and now U.S. Pat. No. 6,179,983, and Contolini et al., co-filed application Ser. No. 08/970,120, filed Nov. 13, 1997, and now U.S. Pat. No. 6,159,354, all of which are incorporated herein by reference in their entirety. This Application is a continuation of Ser. No. 08/969,196 filed Nov. 13, 1997, now U.S. Pat. No. 6,126,798.

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Continuations (1)
Number Date Country
Parent 08/969196 Nov 1997 US
Child 09/574666 US