Ozonated DI water process for organic residue and metal removal processes

Information

  • Patent Grant
  • 6399513
  • Patent Number
    6,399,513
  • Date Filed
    Thursday, September 21, 2000
    23 years ago
  • Date Issued
    Tuesday, June 4, 2002
    22 years ago
Abstract
A method for resist strip and metal contamination removal. Wafers (108) with a patterned resist formed thereon are subjected to an ozonated deionized water solution, such as mist (120). The ozonated deionized water solution (120) strips the resist and removes the resist residue. At the end of the process, HCl (152) is added to the deionized water (116) prior to forming the ozonated deionized water solution (120) to remove metal contaminants.
Description




CROSS-REFERENCE TO RELATED APPLICATIONS




The following co-pending applications are related and are hereby incorporated by reference:




















Serial No.




Filing Date




Inventors













09/667,154




09/21/2000




Jung et al.







09/666,974




09/21/2000




Jung et al.







09/666,576




09/21/2000




Murphy et al.















FIELD OF THE INVENTION




The invention is generally related to the field of resist patterning of semiconductor devices and more specifically to resist strip and metal removal processes.




BACKGROUND OF THE INVENTION




In the fabrication of semiconductor devices, photoresist patterns are routinely used for delineating certain areas of the semiconductor device, for example, for patterned etching and ion implantation. After the etch or implantation sequence, the resist pattern must be removed. This is referred to as a resist strip. Additionally, any resist residue must also be removed. Currently, an ozonated H


2


SO


4


operated at 130° C. or a combined solution of H


2


SO


4


and H


2


O


2


are widely used for resist strip. To reduce particles, the above resist strip process is followed by a SC1 (H


2


O:NH


4


OH:H


2


O


2


) megasonic cleanup. Alternatively, a deionized water (DIW) scrub may be used for particle removal.




Unfortunately, the chemicals described above for resist strip are not environmentally safe and require special precautions for handling and disposal. Furthermore, sulfur compounds have been found to be left on wafer surfaces after the H


2


SO


4


cleanups, which may cause corrosions or work function shifts on devices. The SC1 clean-up may result in NH


3


abatement. If the alternative DIW scrub is used, two process tools are required. Accordingly, a resist strip and particle removal process is desired that is environmentally safe and overcomes the above mentioned particle removal problems.




U.S. Pat. No. 5,464,480 describes a process for removing organic materials such as photoresist without the use of H


2


SO


4


and H


2


O


2


. Wafers are placed in a tank containing chilled deionized water. Ozone is diffused into the chilled deionized water to oxidize the organic material from the wafer surface. This process requires the addition of a chiller to current process equipment.




SUMMARY OF THE INVENTION




The invention is a method and apparatus for resist pattern strip and metal removal that uses an ozonated deionized water with HCl spiking at the end of the process for metal contamination removal. An advantage of the invention is providing a ozonated deionized water resist strip that results in reduce metal contamination and that is environmentally safe.




This and other advantages will be apparent to those of ordinary skill in the art having reference to the specification in conjunction with the drawings.











BRIEF DESCRIPTION OF THE DRAWINGS




In the drawings:





FIG. 1

is a diagram of an apparatus for removing a resist pattern and resist residue according to the invention;





FIG. 2

is a diagram of an ozone delivery system for use with the apparatus of

FIG. 1

;





FIG. 3

is a cross-sectional diagram of a semiconductor wafer having a resist pattern formed thereon;





FIG. 4

is a cross-section diagram of the semiconductor wafer of

FIG. 4

after resist strip and particle removal according to the invention;





FIG. 5

is a graph of a ToF-SIMS surface residue analysis after a source/drain patterning step without the HCl spiking of the invention;




FIG.


6


. is a graph of a ToF-SIMS surface residue analysis after a threshold voltage implant patterning step without the HCl spiking of the invention; and





FIG. 7

is a graph of a ToF-SIMS surface residue analysis after a source/drain pattern ash step comparing the HCl spiking of the invention to an ozonated DIW resist strip process without HCl spiking.











DETAILED DESCRIPTION OF THE EMBODIMENTS




The process of the present invention uses ozonated deionized water (DIW) for resist strip and HCl spiking at the end of the process for metal contamination removal. Elevated temperatures were found to result in an enhanced resist strip rate. Optimum temperatures were found to be in the range of 55-65° C. Residual analysis has showed that ozonated DI water has better removal efficiency on organic compounds. However, an increase in metal contamination was found without the use of HCl spiking at the end of the process. The process of the present invention eliminates the use of hazardous chemicals in positive resist strip and resist residue removal processes.




Because the use of a fine mist spray versus an immersion process was found to increase the resist strip rate approximately 10×, the process of the invention will be described in conjunction with a fine mist spray of ozonated DIW. However, it will be apparent to those of ordinary skill in the art that the benefits of HCl spiking according to the invention may be applied to other methods of applying ozonated DIW such as those described in co-pending U.S. patent applications Ser. Nos. 09/667,154 filed Sep. 21, 2000 and 09/666,974, filed Sep. 21, 2000.




An apparatus


100


according to an embodiment of the invention for resist strip is shown in FIG.


1


. Apparatus


100


comprises a process chamber


102


. Process chamber


102


may be similar to those currently used in spray tools such as the FSI Saturn® by FSI International. Process chamber


102


includes a carrier


104


for holding wafers


108


to be processed. Carrier


104


may be rotated either clockwise or counterclockwise by motor


106


. Drain


110


is located at the bottom of process chamber


102


for draining spent process liquid (e.g., deionized water). An exhaust


112


is also included to allow gases, such as ozone, to exit the process chamber


102


.




Process chamber


102


also includes an atomizer


114


. Deionized water (DIW)


116


and ozone gas


118


are separately added to atomizer


114


. As streams of DIW


116


exit atomizer


114


, jets of ozone gas


118


hit the DIW


116


and atomizes the DIW into a fine mist


120


of ozonated DIW. DIW


116


flow may be controlled using a needle valve. Fine mist


120


is sprayed onto the wafers


108


while the wafers


108


are being rotated. A spray mist of ozonated DIW


120


was found to increase the resist strip rate by approximately 10 times the resist strip rate of an immersion method. In addition, less ozone is needed because saturation of ozone concentration can be achieved more easily using atomizer


114


to pressurize DIW


116


and ensure fine mixing of DIW


116


and ozone


118


in a closed system.




Improved removal rates have been found using elevated temperatures. Therefore, DIW


116


may optionally be heated prior to mixing the DIW


116


with ozone


118


. For example, DIW


116


may be heated to a temperature in the range of 55-65° C. Methods for heating a liquid such as DIW


116


are known in the art. In addition, the chamber lid


150


may be heated. Heating the ozone gas


118


has not been found to be effective in improving the removal rates. In one embodiment of the invention, the DIW


116


is heated for resist stripping, but room temperature DIW


116


is used for residue removal.




A suitable ozone delivery system


123


is shown in

FIG. 3. O



2


/O


3


gas


122


is supplied to two-way valve


124


. Valve


124


is normally open to exhaust. Two-way valve


124


may be actuated to supply ozone gas to atomizer


114


. The ozone gas may be vented to exhaust and then switched to atomizer


114


when the ozone concentration has reached a predetermined concentration. The concentration can be monitored using a gas phase ozone concentration monitor


137


. When ozone gas


122


is supplied to atomizer


114


, valve


130


is closed. A separate chamber purge line


126


is used to supply a purge gas


128


such as N


2


to the atomizer


114


. The purge gas


128


is connected to a N


2


filter and normally opened valve


130


. When it is desirable to purge the system, two-way valve


124


is de-actuated to allow gas (e.g.


122


) to be exhausted. Valve


130


is, in turn, opened, to allow purge gas


128


to be supplied to atomizer


114


. O


2


(and possibly N


2


or other inert gases) is used to purge line


122


and through two-way valve


124


to exhaust


136


when desired.




After being applied to wafer


108


, the ozonated DIW spray


120


is preferably not recirculated. Thus, no filter is needed in a recirculation loop. The single pass of chemicals on the wafer


108


results in lower incidence of wafer-to-wafer or lot-to-lot cross-contamination.




In operation, a number of wafers


108


are loaded into carrier


104


and placed in process chamber


102


. HCl


152


is stored in a pressurized canister


150


and added to the DIW


116


flow prior to entry of the DIW


116


to atomizer


114


during at least a portion of the process. HCl


152


may be added to room temperature or warm DIW


116


. DIW


116


(with or without HCl spiking) and ozone gas


118


are separately added to atomizer


114


. Ozone gas


118


may be supplied at a rate on the order of 50 g/m


3


. Atomizer


114


causes jets of ozone gas


118


to hit (and atomize) streams of DIW


116


to form a fine mist spray


120


of ozonated DIW. Ozonated DIW mist


120


is applied to wafers


108


while the wafers


108


are rotated within process chamber


102


. Rotating the wafers


108


results in a uniform application of ozonated DIW mist


120


. Use of both clockwise and counterclockwise rotation of wafers


108


can further improve the uniformity.




Applying an ozonated DIW mist


120


strips a resist pattern and any resist residue from the surface of wafers


108


. A fine mist spray


120


of ozonated DIW was found to have a 10× improvement in the resist strip rate versus an immersion process.

FIG. 3

shows wafer


108


prior to application of a warm ozonated DIW mist spray


120


.

FIG. 3

is a cross-sectional diagram of wafer


108


with resist pattern


140


and resist residue


142


formed thereon. Resist pattern


140


may included an optional adhesion promoter


141


such as HMDS (hexamethyldisilazane). As shown in

FIG. 3

, resist pattern


140


may be used as a pattern for etching layer


144


. Alternatively, resist pattern


140


may have been used for other purposes, such as ion implanting. Resist patterns, such as pattern


140


are used throughout the semiconductor fabrication process for forming patterned structures, masking implants, etc. During an etch process, for example, resist residue


142


may form on the exposed surface of the etched layer or layers


144


.

FIG. 4

shows wafer


108


after resist strip and resist residue removal according to the invention. The resist strip and residue removal process of the invention is also effective in removing adhesion promoters, such as HMDS.




Without the addition of HCl, higher levels of metal contamination can occur versus a prior art H


2


SO


4


and H


2


O


2


clean.

FIG. 5

is a graph of a ToF-SIMS surface residue analysis for various contaminants after a source/drain patterning and ash step. Metal (Al) contamination was much higher for ozonated DIW both at room temperature and at elevated temperatures than for a H


2


SO


4


and H


2


O


2


clean.

FIG. 6

is a similar graph for contaminants after a patterned p-type threshold adjust implant and ash.




Accordingly, HCl spiking to the ozonated DIW mist


120


may be added at the end of the process to reduce metal contamination. For example, HCl may be added to the DIW


116


flow during the entire contamination removal portion of the process (but not during the earlier resist strip portion).

FIG. 7

is a graph of a ToF-SIMS analysis for various contaminants after a patterned source/drain implant ash step. Adding 150 sccm of HCl significantly reduces metal contamination. The duration of HCl spiking can be tailored depending on the amount of metal contamination expected. A typical duration is on the order of 3 minutes. In the preferred embodiment, HCl is added to the DIW


116


flow at a ratio of 5:1 (DIW:HCl).




For further metal contamination removal, the above process may be followed by a SC2 (H


2


O:HCl:H


2


O


2


) rinse.




While this invention has been described with reference to illustrative embodiments, this description is not intended to be construed in a limiting sense. Various modifications and combinations of the illustrative embodiments, as well as other embodiments of the invention, will be apparent to persons skilled in the art upon reference to the description. For example, other methods for forming and applying spray mist


120


, such as in a single wafer environment, may be used. It is therefore intended that the appended claims encompass any such modifications or embodiments.



Claims
  • 1. A method for fabricating an integrated circuit, comprising the steps of:providing a semiconductor wafer with a resist pattern formed thereon; spraying an ozonated deionized water solution to a surface of said semiconductor wafer to remove said resist pattern; and continuing said step of spraying the ozonated deionized water solution while adding HCl to said ozonated deionized water solution to remove metal contaminants from said surface, wherein said HCl is added to the ozonated deionized water solution only after removing said resist pattern and not during removal of said resist pattern.
  • 2. The method of claim 1, wherein said ozonated deionized water solution has an elevated temperature in the range of 55 to 65° C.
  • 3. The method of claim 1, wherein said ozonated deionized water solution is a spray mist is formed by combining deionized water with ozone in an atomizer.
  • 4. A method for fabricating an integrated circuit, comprising the steps of:providing a semiconductor wafer with a resist pattern formed thereon; spraying an ozonated deionized water solution to a surface of said semiconductor wafer to remove said resist pattern, wherein said ozonated deionized water solution is a spray mist is formed by combining deionized water with ozone in an atomizer; and after removing said resist pattern, continuing said step of spraying the ozonated deionized water solution while adding HCl to said ozonated deionized water solution to remove metal contaminants from said surface, wherein said step of adding HCl adds HCl to said deionized water prior to supplying said deionized water to said atomizer.
  • 5. The method of claim 4, wherein a ratio of deionized water to HCl is on the order of 5:1.
  • 6. The method of claim 1, further comprising the step of rotating said semiconductor wafer during said spraying step.
  • 7. The method of claim 6, wherein said step of rotating said semiconductor wafer comprises alternately rotating said semiconductor wafer in a clockwise direction and a counterclockwise direction.
  • 8. The method of claim 1, wherein said step of adding HCl has a duration on the order of 3 minutes.
  • 9. The method of claim 1, wherein said step of adding HCl adds approximately 150 sccm of HCl.
Parent Case Info

This application claims priority under 35 USC §119(e)(1) of provisional application No. 60/165,149 filed Nov. 12, 1999.

US Referenced Citations (9)
Number Name Date Kind
5776296 Matthews Jul 1998 A
5882489 Bersin et al. Mar 1999 A
6009888 Ye et al. Jan 2000 A
6130169 Shields et al. Oct 2000 A
6143637 Yagi Nov 2000 A
6158445 Olesen et al. Dec 2000 A
6183942 Kim et al. Feb 2001 B1
6191086 Leon et al. Feb 2001 B1
6200736 Tan Mar 2001 B1
Provisional Applications (1)
Number Date Country
60/165149 Nov 1999 US