USRE36006E - Metal selective polymer removal - Google Patents
Metal selective polymer removal Download PDFInfo
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- USRE36006E USRE36006E US08/739,885 US73988596A USRE36006E US RE36006 E USRE36006 E US RE36006E US 73988596 A US73988596 A US 73988596A US RE36006 E USRE36006 E US RE36006E
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- 229910052751 metal Inorganic materials 0.000 title claims abstract description 27
- 239000002184 metal Substances 0.000 title claims abstract description 27
- 229920000642 polymer Polymers 0.000 title claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 53
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 30
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 17
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- 229910009111 xH2 O Inorganic materials 0.000 claims 3
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- 239000012071 phase Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 9
- 235000012431 wafers Nutrition 0.000 description 21
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- 238000006243 chemical reaction Methods 0.000 description 3
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- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
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- 229910015844 BCl3 Inorganic materials 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- STECJAGHUSJQJN-USLFZFAMSA-N LSM-4015 Chemical compound C1([C@@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-USLFZFAMSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
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- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
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- 238000005260 corrosion Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
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- 238000012876 topography Methods 0.000 description 1
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- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
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Images
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02041—Cleaning
- H01L21/02057—Cleaning during device manufacture
- H01L21/02068—Cleaning during device manufacture during, before or after processing of conductive layers, e.g. polysilicon or amorphous silicon layers
- H01L21/02071—Cleaning during device manufacture during, before or after processing of conductive layers, e.g. polysilicon or amorphous silicon layers the processing being a delineation, e.g. RIE, of conductive layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31127—Etching organic layers
- H01L21/31133—Etching organic layers by chemical means
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
- H01L21/321—After treatment
- H01L21/3213—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer
- H01L21/32139—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer using masks
Definitions
- the resist is somewhat more difficult to remove with diffusion enhanced silylated resist processes as compared with conventional processes as a result of larger amounts of etch byproducts such as sidewall polymer (SWP) on vertical walls of a device undergoing fabrication.
- etch byproducts such as sidewall polymer (SWP) on vertical walls of a device undergoing fabrication.
- SWP sidewall polymer
- These byproducts are generally comprised of a metal and SiO 2 molecule.
- the molecule can comprise carbon from the photoresist, metal from the metal layer and SiO 2 .
- sidewall polymer is comprised of aluminum silicate and very small amounts of fluorocarbons. Fluorocarbons are noncombustible and therefore are not removed during an O 2 in-situ ash sequence of a metal etch.
- a process to remove the sidewall polymer without metal lift-off is disclosed.
- FIGS. 1 through 6 are drawings in which applicable reference numerals have been carried forward, which illustrate cross-sectional views of a semiconductor wafer undergoing fabrication according to a diffusion enhanced silyated resist process.
- M2 Metal 2
- TiW titanium tungsten
- W tungsten
- FIGS. 1 through 6 illustrate cross-sectional views of a semiconductor wafer 1 undergoing fabrication according to a diffusion enhanced silylated resist process, that process is as follows.
- a positive resist such as a novolac-based resist 2 is conventionally spin-coated and after subsequent exposure through mask 4, resist 2 is treated with hexamethyldisilazine vapor (HMDS) prior to development.
- HMDS hexamethyldisilazine vapor
- the silyation reaction modifies the surface of the exposed resist, yielding areas 6 which are less susceptible to dry etching by O 2 plasmas. This reverses the normal development behavior of the resist and affords a negative image.
- a main advantage of dry etching the unexposed (and hence underivatized) resist is that it circumvents the undesirable swelling and the concomitant loss of resolution that often accompanies wet etch development. As shown in FIG. 3, an oxygen plasma etch etches away the unexposed resist.
- the wafer is dry etched with an anisotropic reactive ion etching (RIE).
- RIE reactive ion etching
- the chemistries used are Cl 2 /BCl 3 to etch the aluminum alloy followed by SF 6 /Ar to etch the W and TiW. Fine line geometries with essentially vertical walls are ideally obtained as shown in FIG. 4.
- the final step in the etch is an in situ ash which reduces corrosion by oxidizing the responsible chlorine-containing compounds and removes areas 6 which function as bulk resist masks. This etch is greater than 20:1 selective to the SiO 2 substrate.
- the etch is anisotropic because during the process a nonvolatile polymer (SWP) is deposited on the surfaces being etched which protects the underlying surfaces against etching by reactive gas. Stripping of remaining resist and SWP is the last step in the process flow for this level.
- the invention's process is a vapor phase process which involves anhydrous HF and N 2 H x where x is a real number (N 2 H x is achievable by passing nitrogen over water), introduced in a chamber with the wafer to be processed, which react to make the etch byproducts 5 water soluble. After the byproducts acquire their water soluble property, water is applied to the wafer so as to rinse the byproduct away, as shown in FIG. 5.
- aqueous HF can be substituted for anhydrous HF- i.e. one can make vapor HF from aqueous HF and react it with the aforementioned N 2 +H 2 O.
- Vapor phase processing provides an advantage or other types of processing in that it will not corrode metal like aqueous phase or liquid phase processing.
- Experimental data indicates that after processing according to the invention, the sheet resistance on the metal does not change, thereby indicating the reactions during processing do not harm metal. Further, damage resulting from processing to the silicon dioxide substrate can be controlled through the regulation of vapor.
- the process of the invention can be accomplished using a wafer vapor phase cleaner.
- a wafer vapor phase cleaner is a machine that removes oxides from a wafer.
- Wafer vapor phase cleaners include the Advantage, Equinox and . .Excaliber.!. .Iadd.Excalibur® .Iaddend.machines and a vapor HF tool, VPC-811-A by DNS.
- a wafer vapor phase cleaner to remove byproducts of the type discussed above. Cost savings from the invention's process is expected at this time to be approximately 0.03 cents per wafer as compared with current solvent processing methods which incur costs of around $1.50 per wafer.
- there is a safety advantage associated with the invention in that there is virtually no waste disposal as compared with solvents which incidently cannot be diluted.
- a wafer vapor phase cleaner such as an . .Excaliber,.!. .Iadd.Excalibur® .Iaddend.wafers that have been processed according to diffusion enhanced silylated resist processes are etched in a sealed etch chamber and then transported to the rinse position by moving the chamber vertically to expose the rinse cavity of the wafer vapor phase cleaner.
- the two separate process' for the etch and the rinse positions are as follows:
- etch and rinse recipes are exemplary only and that a more or less optimized process recipe may not use the same recipes.
- FIG. 6 illustrates a cross-sectional drawing of stack 8 upon which the DMD is formed.
- This stack comprises bulk semiconductor layer 9, CMOS addressing circuitry 10, photoresist layer 12, and metal layer 14.
- FIG. 7 illustrates a cross-sectional view of a partially formed DMD device
- etching of metal layer 14, shown in FIG. 6, according to well known DMD formation techniques results in the formation of hinges 16 connected to mirrors 18.
- Hinges 16 are connected to metal posts 20 which are formed through vias which extend down to the level of the CMOS addressing circuitry 10 (as shown by the hidden lines).
- Reference numerals 21 represent sidewall polymer which results during the fabrication of the DMD device.
- FIG. 8 illustrates a cross-sectional view of a completed DMD device according to the invention's process
- the invention's sidewall polymer removal process is used to eliminate sidewall polymer 21, thereby greatly increasing the production yield of the DMD device.
Abstract
A metal selective polymer removal process is disclosed which prevents metal lift-off for use especially suited for ULSI fabrication.
Description
The density of devices fabricated on semiconductor substrates has increased steadily over the years with ultra large scale integration (ULSI) currently being employed in 16 megabit (MB) dynamic random access memories (DRAMs). Accompanying this trend have been decreased feature sizes (currently less than or equal to 0.5 microns) and increased demands on process technology. To pattern such small features, conventional lithographic procedures are being supplanted by newer ones based on diffusion enhanced silylated resist DESIRE™ processes. The numerous reports of the success of the diffusion enhanced silylated processes in producing sub-half micron features in various resists, using one line and deep ultra violet light exposure indicates this process has a bright future. The resolution and throughput rate up to the image transfer step exceeds that of conventional positive resists and are clearly superior when topography is of major concern. The resist is somewhat more difficult to remove with diffusion enhanced silylated resist processes as compared with conventional processes as a result of larger amounts of etch byproducts such as sidewall polymer (SWP) on vertical walls of a device undergoing fabrication. These byproducts, generally referred to as polymers, are generally comprised of a metal and SiO2 molecule. For instance, the molecule can comprise carbon from the photoresist, metal from the metal layer and SiO2. Further, data has indicated that sidewall polymer is comprised of aluminum silicate and very small amounts of fluorocarbons. Fluorocarbons are noncombustible and therefore are not removed during an O2 in-situ ash sequence of a metal etch. Thus, ashing has proven to be ineffective because of the high carbon content in the byproduct molecule from the photoresist. The difficulty with which resist can be removed has proven to be a severe impediment to the generation of sub-half micron features. Previously solvent/ultrasonic agitation had been used to remove SWP. For instance, soaking the device undergoing fabrication in an ethanolamine solution followed optionally with ultrasonic agitation using a Ney ultrasonic (which allows the capability of adjusting the power of the ultrasonic) has been used in the past. However, these techniques prove to be unusable because of the tendency of metal, such as aluminum, to lift off of the minimum features. Further, these techniques tend to leave behind significant amounts of residue on device sidewalls and on device surfaces. Until now, no effective means has been available to solve the problem of removing sidewall polymer resulting from diffusion enhanced silyated resist processes.
A process to remove the sidewall polymer without metal lift-off is disclosed.
FIGS. 1 through 6 are drawings in which applicable reference numerals have been carried forward, which illustrate cross-sectional views of a semiconductor wafer undergoing fabrication according to a diffusion enhanced silyated resist process.
Late in the fabrication sequence, specific devices such as DRAMs must be electrically interconnected to accomplish the desired circuit function. One important aspect of this interconnection concerns the second interconnect level and the last level in the manufacture of the device, conventionally known as Metal 2 (M2). The M2 scheme as shown in the cross-sectional FIG. 1, conventionally comprises a Si O2 substrate followed by metal 2 which generally comprises a layer of titanium tungsten (TiW) under tungsten (W) which lies under aluminum alloy which includes 1% silicon and 0.5% copper. With reference to FIGS. 1 through 6 which illustrate cross-sectional views of a semiconductor wafer 1 undergoing fabrication according to a diffusion enhanced silylated resist process, that process is as follows. A positive resist such as a novolac-based resist 2 is conventionally spin-coated and after subsequent exposure through mask 4, resist 2 is treated with hexamethyldisilazine vapor (HMDS) prior to development. The silyation reaction modifies the surface of the exposed resist, yielding areas 6 which are less susceptible to dry etching by O2 plasmas. This reverses the normal development behavior of the resist and affords a negative image. A main advantage of dry etching the unexposed (and hence underivatized) resist is that it circumvents the undesirable swelling and the concomitant loss of resolution that often accompanies wet etch development. As shown in FIG. 3, an oxygen plasma etch etches away the unexposed resist. In order to transfer the pattern into the metal, the wafer is dry etched with an anisotropic reactive ion etching (RIE). The chemistries used are Cl2 /BCl3 to etch the aluminum alloy followed by SF6 /Ar to etch the W and TiW. Fine line geometries with essentially vertical walls are ideally obtained as shown in FIG. 4. The final step in the etch is an in situ ash which reduces corrosion by oxidizing the responsible chlorine-containing compounds and removes areas 6 which function as bulk resist masks. This etch is greater than 20:1 selective to the SiO2 substrate. The etch is anisotropic because during the process a nonvolatile polymer (SWP) is deposited on the surfaces being etched which protects the underlying surfaces against etching by reactive gas. Stripping of remaining resist and SWP is the last step in the process flow for this level. The invention's process is a vapor phase process which involves anhydrous HF and N2 Hx where x is a real number (N2 Hx is achievable by passing nitrogen over water), introduced in a chamber with the wafer to be processed, which react to make the etch byproducts 5 water soluble. After the byproducts acquire their water soluble property, water is applied to the wafer so as to rinse the byproduct away, as shown in FIG. 5. Note that aqueous HF can be substituted for anhydrous HF- i.e. one can make vapor HF from aqueous HF and react it with the aforementioned N2 +H2 O. Vapor phase processing provides an advantage or other types of processing in that it will not corrode metal like aqueous phase or liquid phase processing. Experimental data indicates that after processing according to the invention, the sheet resistance on the metal does not change, thereby indicating the reactions during processing do not harm metal. Further, damage resulting from processing to the silicon dioxide substrate can be controlled through the regulation of vapor. The process of the invention can be accomplished using a wafer vapor phase cleaner. A wafer vapor phase cleaner is a machine that removes oxides from a wafer. Wafer vapor phase cleaners include the Advantage, Equinox and . .Excaliber.!. .Iadd.Excalibur® .Iaddend.machines and a vapor HF tool, VPC-811-A by DNS. Until now, no one has used a wafer vapor phase cleaner to remove byproducts of the type discussed above. Cost savings from the invention's process is expected at this time to be approximately 0.03 cents per wafer as compared with current solvent processing methods which incur costs of around $1.50 per wafer. Additionally, there is a safety advantage associated with the invention in that there is virtually no waste disposal as compared with solvents which incidently cannot be diluted.
An exemplary process flow is illustrative of the preferred embodiment of the invention is given below:
In a wafer vapor phase cleaner, such as an . .Excaliber,.!. .Iadd.Excalibur® .Iaddend.wafers that have been processed according to diffusion enhanced silylated resist processes are etched in a sealed etch chamber and then transported to the rinse position by moving the chamber vertically to expose the rinse cavity of the wafer vapor phase cleaner. The two separate process' for the etch and the rinse positions are as follows:
______________________________________ Etch position Step 0 After inserting the wafer into the chamber, the chamber is purged for 5 seconds with nitrogen at 30 liters/minutes (lpm) Step 1 The process nitrogen flow rate is stabilized for 5 seconds at 12 lpm and the chamber pressure is controlled to 26 inches of water column (TWC).Step 2 The water laden nitrogen is added at a flow rate of 2 lpm for 10 seconds. This will allow a thin layer of water to condense on the surface of the wafer.! Step 3 Anhydrous HF is added to the other gases at a flow ratea of 180 cc/minute. The nitrogen flow rates are changed to 16 lpm and 10 lpm for the carrier gas and the water vapor respectively. Total etch time is 5 seconds. Oxides are removed dudring the step leaving non-volatile material on the surface. Step 4 For 15 seconds the chamber is purged with high velocity nitrogen (12 lpm) and water vapor (10 lpm) to stop the reaction from occuring and to purge reactants for the chamber.Step 5,6 Transition steps form etch to rinse position. Rinse Position Step 0 One second to stabilize the position. Step 1 Wafer receives a 10 second deionized water rinse at a spin speed of 100 rpm. Water soluble metal fluorides are removed in this step.Step 2 Discontinue water rinse and allow water on wafer to be removed before ramping up to dry spin speed. Process time is about one minute. Step 3 Ramp to 3000 rpm to dry wafer and increase nitrogen gas flow to 30 lpm. The wafer is dried in 15 seconds. ______________________________________
One example of a process program using an . .Excaliber.!. .Iadd.Excalibur® .Iaddend.system is given below. Note that the etch and rinse recipes are exemplary only and that a more or less optimized process recipe may not use the same recipes.
______________________________________ Excalibur Process Step Time N.sub.2 A Vapor HF-1 HF-2 N.sub.2 B VSB H.sub.2 O T.T. # Sec lpm lpm sccm sccm lpm 0/1 0/1 RPM ______________________________________ Etch Process 0 5 30.0 1.0 0 0 20 1 5 12.0 1.0 0 0 20 2 10 12.0 2.0 1.0 0 0 20 3 5 16.0 10.0 180 0 1.0 0 0 20 4 15 22.0 2.0 1.0 0 0 20 5 1 6.0 1.0 0 0 20 6 1 6.0 1.0 0 0 20 Rinse Position R0 1 6.0 1.0 0 0 20R1 10 6.0 1.0 0 0 1000 R2 1 6.0 1.0 0 0 1000 R3 15 30.0 1.0 0 0 3000 Etch Position 7 1 30.0 2.0 0 0 20 ______________________________________
One application with which the foregoing described process can be used concerns deformable mirror devices (DMDs). FIG. 6 illustrates a cross-sectional drawing of stack 8 upon which the DMD is formed. This stack comprises bulk semiconductor layer 9, CMOS addressing circuitry 10, photoresist layer 12, and metal layer 14. With reference to FIG. 7 which illustrates a cross-sectional view of a partially formed DMD device, etching of metal layer 14, shown in FIG. 6, according to well known DMD formation techniques results in the formation of hinges 16 connected to mirrors 18. Hinges 16 are connected to metal posts 20 which are formed through vias which extend down to the level of the CMOS addressing circuitry 10 (as shown by the hidden lines). Reference numerals 21 represent sidewall polymer which results during the fabrication of the DMD device. An even greater presence of sidewall polymer 21 can exist after etch away of photoresist layer 12. The sidewall polymer presents particularly annoying problems for DMD functionality in that it can interfere with the swiveling (into or out of the page) of mirrors 18 so that they can make contact with CMOS addressing circuitry 10 after layer 12 is removed. With reference to FIG. 8, which illustrates a cross-sectional view of a completed DMD device according to the invention's process, after layer 12 of FIG. 7 is removed, the invention's sidewall polymer removal process is used to eliminate sidewall polymer 21, thereby greatly increasing the production yield of the DMD device.
Although the invention has been described in detail herein with reference to its preferred embodiment and certain described alternatives, it is to be understood that this description is by way of example only, and it is not to be construed in a limiting sense. Although the invention has been described in some aspects as referring to a DESIRE™ process, it is to be understood that the foregoing invention can be used with any photoresist process. It is to be further understood that numerous changes in the details of the embodiments of the invention, and additional embodiments of the invention, will be apparent to, and may be made by, persons of ordinary skill in the art having reference to this description. It is contemplated that all such changes and additional embodiments are within the spirit and true . .scop.!. .Iadd.scope .Iaddend.of the invention as claimed below.
Claims (15)
1. A process for removal of . .metal etch.!. byproducts .Iadd.from a metal etch .Iaddend.from a semiconductor wafer comprising the following steps:
introducing HF into a chamber containing said wafer which includes non-water soluble byproducts thereon;
introducing N2 +xH2 O, where x is a real number, into said chamber; and
removing soluble byproducts from said wafer after performing the above steps.
2. A process as recited in claim 1 where HF is anhydrous.
3. A process for removing post etch metal silicate-containing residue from a metal structure comprising the following steps:
introducing vapor HF into a chamber containing said metal structure which includes non water soluble residue thereon;
passing a gas over water and introducing the result into said chamber; and
removing said post etch metal silicate-containing residue from said structure after performing the above steps.
4. A process as recited in claim 1 wherein said HF is vapor HF made . .form.!. .Iadd.from .Iaddend.aqueous HF.
5. A process as recited in claim 1 which is performed within a wafer . .vapos.!. .Iadd.vapor .Iaddend.phase cleaner.
6. A process for removing sidewall polymer from the posts of a deformable mirror device comprising the following steps:
introducing HF into a chamber containing said device which includes non-water soluble byproducts thereon,
introducing N2 +xH2 O, where x is a real number, into said chamber; and
removing soluble byproduct from said device after performing the above steps.
7. A process as recited in claim 6 which is performed within a vapor phase cleaner.
8. A process for removing post etch residue from a metal structure comprising the following steps:
introducing anhydrous HF into a chamber containing said metal structure which includes non water soluble residue thereon;
introducing water vapor into said chamber; and
removing said post .Iadd.etch .Iaddend.residue from said structure after performing the above steps.
9. A process as recited in claim 8 wherein the removal of said post etch residue includes rinsing said structure with water.
10. A process for removing post etch residue from a metal structure comprising the following steps:
introducing anhydrous HF into a chamber containing said metal structure which includes non water soluble residue thereon;
passing a gas over water and introducing the result into said chamber; and
removing said post etch residue from said structure after performing the above steps.
11. A process as recited in claim 10 wherein the removal of said post etch residue includes rinsing said structure with water.
12. A process as recited in claim 10 wherein said gas is nitrogen.
13. A process as recited in claim 3 wherein said gas is nitrogen.
14. A process as recited in claim 3 wherein the removal of said post etch residue includes rinsing said structure with water. .Iadd.
15. The process of claim 1 wherein the removing of the soluble byproducts includes rinsing the wafer with water..Iaddend..Iadd.16. The process of claim 1 whereby the introducing HF and N2 +xH2 O further comprises chemically reacting the non-soluble byproducts so as to form water soluble byproducts..Iaddend..Iadd.17. The process of claim 1 wherein the byproducts comprise carbon and metal..Iaddend..Iadd.18. The process of claim 8 whereby the introducing the anhydrous HF step and the introducing water vapor step further comprises chemically reacting the non-soluble residue so as to form water soluble residue prior to removing the residue..Iaddend..Iadd.19. The process of claim 10 whereby the introducing the anhydrous HF step and the introducing water vapor step further further comprises chemically reacting the non-soluble residue so as to form water soluble residue prior to removing the residue..Iaddend.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/739,885 USRE36006E (en) | 1992-09-03 | 1996-10-31 | Metal selective polymer removal |
Applications Claiming Priority (2)
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US07/940,101 US5348619A (en) | 1992-09-03 | 1992-09-03 | Metal selective polymer removal |
US08/739,885 USRE36006E (en) | 1992-09-03 | 1996-10-31 | Metal selective polymer removal |
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US07/940,101 Reissue US5348619A (en) | 1992-09-03 | 1992-09-03 | Metal selective polymer removal |
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ID=25474228
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US07/940,101 Ceased US5348619A (en) | 1992-09-03 | 1992-09-03 | Metal selective polymer removal |
US08/739,885 Expired - Lifetime USRE36006E (en) | 1992-09-03 | 1996-10-31 | Metal selective polymer removal |
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US07/940,101 Ceased US5348619A (en) | 1992-09-03 | 1992-09-03 | Metal selective polymer removal |
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EP (1) | EP0585936B1 (en) |
JP (1) | JPH077002A (en) |
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DE (1) | DE69334049T2 (en) |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US6174817B1 (en) * | 1998-08-26 | 2001-01-16 | Texas Instruments Incorporated | Two step oxide removal for memory cells |
US20040084413A1 (en) * | 1999-01-27 | 2004-05-06 | Matsushita Electric Industrial Co., Ltd. | Etching method |
US7341117B2 (en) | 2001-11-14 | 2008-03-11 | Halliburton Energy Services, Inc. | Method and apparatus for a monodiameter wellbore, monodiameter casing, monobore, and/or monowell |
US20050142880A1 (en) * | 2003-12-27 | 2005-06-30 | Park Tae W. | Polymer removal method for use in manufacturing semiconductor devices |
Also Published As
Publication number | Publication date |
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DE69334049D1 (en) | 2006-09-07 |
EP0585936A2 (en) | 1994-03-09 |
US5348619A (en) | 1994-09-20 |
EP0585936B1 (en) | 2006-07-26 |
TW241387B (en) | 1995-02-21 |
KR100270416B1 (en) | 2000-12-01 |
EP0585936A3 (en) | 1995-03-29 |
JPH077002A (en) | 1995-01-10 |
KR940008000A (en) | 1994-04-28 |
DE69334049T2 (en) | 2007-02-15 |
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