US20030104697A1 - Dry clean method instead of traditional wet clean after metal etch - Google Patents
Dry clean method instead of traditional wet clean after metal etch Download PDFInfo
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- US20030104697A1 US20030104697A1 US10/339,157 US33915703A US2003104697A1 US 20030104697 A1 US20030104697 A1 US 20030104697A1 US 33915703 A US33915703 A US 33915703A US 2003104697 A1 US2003104697 A1 US 2003104697A1
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- 238000000034 method Methods 0.000 title claims abstract description 65
- 229910052751 metal Inorganic materials 0.000 title description 21
- 239000002184 metal Substances 0.000 title description 20
- 239000007789 gas Substances 0.000 claims abstract description 62
- 238000001465 metallisation Methods 0.000 claims abstract description 36
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 26
- 239000011737 fluorine Substances 0.000 claims abstract description 26
- 239000001301 oxygen Substances 0.000 claims abstract description 23
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 23
- 239000000203 mixture Substances 0.000 claims abstract description 22
- 238000012545 processing Methods 0.000 claims abstract description 18
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 17
- 238000005108 dry cleaning Methods 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 239000004065 semiconductor Substances 0.000 claims abstract description 6
- 230000004888 barrier function Effects 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 18
- 229910000838 Al alloy Inorganic materials 0.000 claims description 17
- 238000004140 cleaning Methods 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000008367 deionised water Substances 0.000 claims description 11
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- 239000000758 substrate Substances 0.000 claims description 6
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- 238000006243 chemical reaction Methods 0.000 description 8
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- 230000007797 corrosion Effects 0.000 description 8
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- 239000006227 byproduct Substances 0.000 description 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 5
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 5
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- 239000000463 material Substances 0.000 description 4
- 238000002161 passivation Methods 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
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- 150000002500 ions Chemical class 0.000 description 3
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- 239000000126 substance Substances 0.000 description 3
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- 101100107923 Vitis labrusca AMAT gene Proteins 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000004380 ashing Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 238000011143 downstream manufacturing Methods 0.000 description 2
- 238000001312 dry etching Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
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- 238000011160 research Methods 0.000 description 2
- -1 silicon halide Chemical class 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910017107 AlOx Inorganic materials 0.000 description 1
- 229910015844 BCl3 Inorganic materials 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910016553 CuOx Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910003087 TiOx Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
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- 239000011651 chromium Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
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- 238000011065 in-situ storage Methods 0.000 description 1
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- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
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- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- HLLICFJUWSZHRJ-UHFFFAOYSA-N tioxidazole Chemical compound CCCOC1=CC=C2N=C(NC(=O)OC)SC2=C1 HLLICFJUWSZHRJ-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
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 potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table 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
- H01L21/32133—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only
- H01L21/32135—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only
- H01L21/32136—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only using plasmas
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S134/00—Cleaning and liquid contact with solids
- Y10S134/902—Semiconductor wafer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S438/00—Semiconductor device manufacturing: process
- Y10S438/906—Cleaning of wafer as interim step
Definitions
- passivation formation of the sidewall polymer within the etched structure
- an adequate passivation step followed by a poor clean step will also cause pitting and corrosion.
- device dimensions, or design rule getting smaller and smaller, the influence of any such defects on device performance and reliability is becoming greater and greater.
- a further problem is the ring type residue, or when a high Rc occurs at the wafer edge due to penetration of TiN from an ACT wet clean.
- metal corrosion can occur that is caused by the reaction of chlorine gas and humidity to form HCl acid.
- U.S. Pat. No. 4,501,061 to Wonnacott et al. describes a method for stripping an organic photoresist layer from a semiconductor device using CF 4 and O 2 plasma.
- the photoresist layer is oxidized with oxygen plasma and residual sulfur species are subsequently removed using a fluorine-containing plasma.
- U.S. Pat. No. 5,378,653 to Yanagida describes a method of forming an Al-based pattern whereby dry etching with high selectively of an Al-based metallization layer and effective preventive measures for after-corrosion can be realized. If after etching residual chlorine is removed by O 2 plasma ashing or plasma processing using a fluorine based gas, durability to after-corrosion can be improved further.
- U.S. Pat. No. 5,599,743 to Nakagawa et al. describes a method of manufacturing a semiconductor device that includes etching an aluminum or alloy film through a mask by chlorination and/or bromination with plasma. The film is exposed to either: a gas plasma not liable to deposit or oxidize, but capable of substituting fluoride for chloride and/or bromide; or a gas mixture plasma comprising hydrogen and the above mentioned gas. The device is then washed with water and the mask is removed.
- U.S. Pat. No. 5,976,986 to Naeem et al. describes a low pressure and low power Cl 2 /HCl process for sub-micron metal etching.
- Cl 2 and HCl are used as reactant species by creating a transformer coupled plasma with power applied to electrodes positioned both above and below a substrate with metallization thereon to be etched.
- Three layer metallizations which include bulk aluminum or aluminum alloy sandwiched between barrier layers made from, for example, Ti/TiN, are etched in a three step process wherein relatively lower quantities of Cl 2 are used in the plasma during etching of the barrier layers and relatively higher quantities of Cl 2 are used during etching of the bulk aluminum or aluminum alloy layer.
- the ratio of etchants Cl 2 and HCl and an inert gas, such as N 2 , are controlled in a manner such that a very thin sidewall layer (10-100 ⁇ ) of reaction byproducts during RIE are deposited on the sidewalls of trenches within the etched metallization.
- the process does not use magnetic fields during etching.
- U.S. Pat. No. 5,908,319 to Xu et al. describes forming a microwave plasma in a microwave downstream process from a gas that has a small quantity of fluorine to enhance ashing without substantial oxide loss. This process may be performed before or after other microwave downstream processes or reactive ion etching processes.
- U.S. Pat. No. 5,795,831 to Nakayama et al. describes a method of removing a resist layer including a reactive ion etch (RIE) process and a downstream microwave process each performed at a wafer temperature no greater than about 60° C.
- RIE reactive ion etch
- the low temperature precludes having to pre-heat the resist to drive off solvents.
- U.S. Pat. No. 6,017,826 to Zhou et al. describes a method for forming a patterned layer within a microelectronics fabrication.
- a first plasma etch method is used to etch a blanket hard mask using an overlying patterned photoresist layer as a first etch mask layer, while exposing a blanket chlorine containing plasma etchable layer.
- a second plasma etch method is used to etch the exposed blanket chlorine containing plasma etchable layer using at least the patterned blanket hard mask layer as a second etch mask layer.
- the second plasma etch sidewall passivation layer is formed upon a sidewall of the patterned chlorine containing plasma etchable layer.
- a third plasma etch method strips the sidewall passivation layer while sequentially oxidizing the sidewall of the patterned chlorine containing plasma etchable layer.
- the third plasma etch method employs a third etchant gas composition which, upon plasma activation, forms an oxygen containing oxidizing species.
- U.S. Pat. No. 5,882,489 to Bersin et al. describes a method for removing a resist while avoiding the use of acids and industrial solvents.
- Plasma is used to remove organic compounds.
- the device is rinsed in deionized water (DI), and it is then sputtered with argon to remove inorganic compounds.
- DI deionized water
- argon argon sputtering
- U.S. Pat. No. 5,578,133 to Sugino et al. describes a dry cleaning process for removing metal contaminants from a surface of an oxide film.
- a reaction area is formed on the oxide film such that a silicon surface is formed corresponding to the reaction area.
- a dry cleaning gas is supplied to the oxide film including the reaction area to produce silicon halide molecules.
- the dry cleaning gas being selected from the group essentially consisting of clorine, bromine, hydrogen chloride, hydrogen bromide, and a mixture thereof.
- the silicon halide molecules so formed are supplied to a surface of the oxide film and metal elements existing on the surface of the oxide film are removed.
- Another object of the present invention is to provide an improved dry cleaning method after metal etch to lower the defect density and engineering repair time.
- an etched metallization structure is provided and placed in a processing chamber.
- the etched metallization structure is cleaned by introducing a fluorine containing gas/oxygen containing gas mixture into the processing chamber proximate the etched metallization structure without the use of a downstream microwave while applying a magnetic field proximate the etched metallization structure and maintaining a pressure of less than about 50 millitorr within the processing chamber for a predetermined time.
- FIGS. 1 through 5 schematically illustrate in cross-sectional representation a preferred embodiment of the present invention.
- FIG. 6 is a cross-sectional representation of the tool that may be used with the present invention.
- FIG. 7A and 7B are top down, plan views of the permissible magnet orientations.
- a conventional aluminum or aluminum alloy metallization typically is comprised of dielectric layer 30 (e.g. ILD, IMD, or oxide), bottom barrier layer 10 , bulk aluminum or aluminum alloy 12 , and upper barrier layer 14 .
- dielectric layer 30 e.g. ILD, IMD, or oxide
- bottom barrier layer 10 e.g., bottom barrier layer 10
- bulk aluminum or aluminum alloy 12 e.g., aluminum or aluminum alloy 12
- upper barrier layer 14 e.g., aluminum or aluminum alloy
- Patterned photoresist layer 16 overlies upper barrier layer 14 .
- Barrier layers 10 , 14 are preferably comprised of an inner Ti layer 10 B, 14 B adjacent bulk aluminum or aluminum alloy 12 , and outer TiN layer 10 A, 14 A facing away from bulk aluminum or aluminum alloy 12 .
- Barrier layers 10 , 14 may also be comprised of other metal or metal alloys such as tantalum, tungsten, molybdenum, chromium, vanadium, niobium, zirconium, or metal-silicon nitrides.
- Barrier layers 10 , 14 are preferably from about 5 to 150 nm thick.
- Bulk aluminum or aluminum alloy 12 is preferably an aluminum copper alloy with 0.5% copper (Al-0.5% Cu or just Al(Cu)).
- Al(Cu) layer 12 is preferably from about 100 to 1500 nm thick.
- Photoresist layer 16 may be comprised of a variety of organic materials, such as Barl 900TM material manufactured by Brewer Science, U.S.A., or Novalic material because they are photosensitive.
- the metallization etch process includes the following parameters: from about 0 to 100 sccm BCl 3 gas flow, from about 0 to 200 sccm Cl 2 gas flow, from about 0 to 20 sccm N 2 gas flow, from about 0 to 20 sccm CH 4 gas flow, and from about 0 to 20 sccm CHF 3 .
- Either a Lam Research model TCP 9600 tool or an AMAT (Applied Materials) model DPS metal tool may be used.
- Polymer layer 20 serves to protect sidewalls 22 from the etchant and preserve the anisotropic nature of the etching, i.e. maintenance of vertical sidewalls 22 .
- the conventional metal stack for aluminum—0.5% copper alloy is photoresist 16 /TiN layer 14 A/Ti layer 14 B/Al(Cu) layer 12 /Ti layer 10 B/TiN layer 10 A/oxide layer 30
- the property of the sidewall polymer 20 that forms over the sidewalls 22 of the etched structure is organic plus oxide-like.
- This polymer 20 is quite a bit stickier on the metal line and sidewall 22 after plasma etching and in-situ photoresist (PR) 16 stripping.
- PR photoresist
- Step I and Step II The inventors have discovered that removing the polymer layer 20 requires the use of a two step process (Step I and Step II):
- STEP I low pressure of less than 50 millitorr, more preferably from about 10 to 50 millitorr, and most preferably about 20 millitorr;
- medium RF power of greater than about 200 W, more preferably from about 200 to 500 W, and most preferably about 300W;
- a magnetic field greater than about 10 gauss (G), more preferably from about 20 to 100 gauss, and most preferably about 20 gauss at a radio frequency of about 13.56 MHz;
- the fluorine containing gas may be CF 4 , NF 3 , or CHF 3 , and is preferably CF 4
- the oxygen containing gas may be O 2, or O 3, and is preferably O 2 .
- DI deionized water
- initial treatment of the structure of FIG. 3 leaves sidewall polymer residue 20 extending over outer TiN layer 14 A.
- FIG. 6 illustrates the major elements of the tool that may be used in the present invention.
- the wafer 60 is supported by an electrode statistic chuck (ESC) 62 within processing chamber 64 .
- RF power source 66 supplies the necessary RF power.
- Processing chamber 64 is flanked by magnetic field 68 .
- FIGS. 7A and 7B illustrate top down, plan views of two permissible magnet 70 A, 70 B, 70 C, 70 D; and 72 A, 72 B, 72 C, and 72 D, respectively, orientations.
- Lam Research model TCP 9600 tool and the AMAT model DPS-metal tool.
- the following tool configurations may also be used: magnetic enhanced RIE and magnetic confinement triode RIE.
- the yield is increased due to the decreased defect density
- fluorine gas is useful for oxide removal (such as TiO x , AlO x , CuO x , and SiO 2 ), and an O 2/ N 2 gas mixture or an H 2 /N 2 gas mixture or both gas mixtures is useful for photoresist layer 16 removal/strip. So it would be anticipated that using fluorine gas with an O 2 /N 2 gas mixture or an H 2 /N 2 gas mixture or both gas mixtures would be useful to strip photoresist layer 16 and to remove sidewall polymer layer 20 .
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Drying Of Semiconductors (AREA)
Abstract
A dry cleaning method for use in semiconductor fabrication, including the following steps. An etched metallization structure is provided and placed in a processing chamber. The etched metallization structure is cleaned by introducing a fluorine containing gas/oxygen containing gas mixture into the processing chamber proximate the etched metallization structure without the use of a downstream microwave while applying a magnetic field proximate the etched metallization structure and maintaining a pressure of less than about 50 millitorr within the processing chamber for a predetermined time.
Description
- Prevention of metal corrosion and pitting defects with conventional wet cleaning methods after metal etching is difficult. Wet cleaning methods can leave chlorine (Cl2) trapped in a thin sidewall polymer which maximizes corrosion and pitting of, for example, an aluminum (Al) or aluminum alloy substrate. If a thicker sidewall polymer is formed to minimize the exposure of the aluminum/aluminum alloy substrate to Cl2, the difficulty of a more narrow window within which to perform the wet clean arises.
- Therefore, passivation (formation of the sidewall polymer within the etched structure) during dry etching and clean step is a critical step. Sometimes an adequate passivation step followed by a poor clean step will also cause pitting and corrosion. With device dimensions, or design rule, getting smaller and smaller, the influence of any such defects on device performance and reliability is becoming greater and greater.
- In high ion density reactors using high power processes, certain problems present. One such problem is a high rate of resist erosion and loss of a substantial amount of substrate dielectric, generally silicon oxide (SiO2). This process also is more prone to corrosion known as “mouse bites” characterized as an undesirable lateral loss of Al(Cu).
- Another problem is that a metal to tungsten (W) galvanic reaction erodes the interface of the metal Al(Cu) and the W stud. This leads to the loss of W and an increased Rc.
- A further problem is the ring type residue, or when a high Rc occurs at the wafer edge due to penetration of TiN from an ACT wet clean.
- Also, metal corrosion can occur that is caused by the reaction of chlorine gas and humidity to form HCl acid.
- U.S. Pat. No. 4,501,061 to Wonnacott et al. describes a method for stripping an organic photoresist layer from a semiconductor device using CF4 and O2 plasma. The photoresist layer is oxidized with oxygen plasma and residual sulfur species are subsequently removed using a fluorine-containing plasma.
- U.S. Pat. No. 5,378,653 to Yanagida describes a method of forming an Al-based pattern whereby dry etching with high selectively of an Al-based metallization layer and effective preventive measures for after-corrosion can be realized. If after etching residual chlorine is removed by O2 plasma ashing or plasma processing using a fluorine based gas, durability to after-corrosion can be improved further.
- U.S. Pat. No. 5,599,743 to Nakagawa et al. describes a method of manufacturing a semiconductor device that includes etching an aluminum or alloy film through a mask by chlorination and/or bromination with plasma. The film is exposed to either: a gas plasma not liable to deposit or oxidize, but capable of substituting fluoride for chloride and/or bromide; or a gas mixture plasma comprising hydrogen and the above mentioned gas. The device is then washed with water and the mask is removed.
- U.S. Pat. No. 5,976,986 to Naeem et al. describes a low pressure and low power Cl2/HCl process for sub-micron metal etching. Cl2 and HCl are used as reactant species by creating a transformer coupled plasma with power applied to electrodes positioned both above and below a substrate with metallization thereon to be etched. Three layer metallizations which include bulk aluminum or aluminum alloy sandwiched between barrier layers made from, for example, Ti/TiN, are etched in a three step process wherein relatively lower quantities of Cl2 are used in the plasma during etching of the barrier layers and relatively higher quantities of Cl2 are used during etching of the bulk aluminum or aluminum alloy layer. The ratio of etchants Cl2 and HCl and an inert gas, such as N2, are controlled in a manner such that a very thin sidewall layer (10-100Å) of reaction byproducts during RIE are deposited on the sidewalls of trenches within the etched metallization. The process does not use magnetic fields during etching.
- U.S. Pat. No. 5,908,319 to Xu et al. describes forming a microwave plasma in a microwave downstream process from a gas that has a small quantity of fluorine to enhance ashing without substantial oxide loss. This process may be performed before or after other microwave downstream processes or reactive ion etching processes.
- U.S. Pat. No. 5,795,831 to Nakayama et al. describes a method of removing a resist layer including a reactive ion etch (RIE) process and a downstream microwave process each performed at a wafer temperature no greater than about 60° C. The low temperature precludes having to pre-heat the resist to drive off solvents.
- U.S. Pat. No. 5,709,757 to Hatano et al. describes a dry clean.
- U.S. Pat. No. 6,017,826 to Zhou et al. describes a method for forming a patterned layer within a microelectronics fabrication. A first plasma etch method is used to etch a blanket hard mask using an overlying patterned photoresist layer as a first etch mask layer, while exposing a blanket chlorine containing plasma etchable layer. A second plasma etch method is used to etch the exposed blanket chlorine containing plasma etchable layer using at least the patterned blanket hard mask layer as a second etch mask layer. The second plasma etch sidewall passivation layer is formed upon a sidewall of the patterned chlorine containing plasma etchable layer. A third plasma etch method strips the sidewall passivation layer while sequentially oxidizing the sidewall of the patterned chlorine containing plasma etchable layer. The third plasma etch method employs a third etchant gas composition which, upon plasma activation, forms an oxygen containing oxidizing species.
- U.S. Pat. No. 5,882,489 to Bersin et al. describes a method for removing a resist while avoiding the use of acids and industrial solvents. Plasma is used to remove organic compounds. The device is rinsed in deionized water (DI), and it is then sputtered with argon to remove inorganic compounds. The order of DI rinsing and argon sputtering may be reversed.
- U.S. Pat. No. 5,578,133 to Sugino et al. describes a dry cleaning process for removing metal contaminants from a surface of an oxide film. A reaction area is formed on the oxide film such that a silicon surface is formed corresponding to the reaction area. A dry cleaning gas is supplied to the oxide film including the reaction area to produce silicon halide molecules. The dry cleaning gas being selected from the group essentially consisting of clorine, bromine, hydrogen chloride, hydrogen bromide, and a mixture thereof. The silicon halide molecules so formed are supplied to a surface of the oxide film and metal elements existing on the surface of the oxide film are removed.
- Accordingly, it is an object of the present invention to provide an improved dry cleaning method after metal etch to prevent metal corrosion and pitting.
- Another object of the present invention is to provide an improved dry cleaning method after metal etch to lower the defect density and engineering repair time.
- It is a further object of the present invention to provide a fluorine containing gas/oxygen containing gas dry cleaning method without a downstream microwave power that uses magnetic power, a relatively low pressure, and medium bias RF power.
- Other objects will appear hereinafter.
- It has now been discovered that the above and other objects of the present invention may be accomplished in the following manner. Specifically, an etched metallization structure is provided and placed in a processing chamber. The etched metallization structure is cleaned by introducing a fluorine containing gas/oxygen containing gas mixture into the processing chamber proximate the etched metallization structure without the use of a downstream microwave while applying a magnetic field proximate the etched metallization structure and maintaining a pressure of less than about 50 millitorr within the processing chamber for a predetermined time.
- The features and advantages of the method of the present invention will be more clearly understood from the following description taken in conjunction with the accompanying drawings in which like reference numerals designate similar or corresponding elements, regions and portions and in which:
- FIGS. 1 through 5 schematically illustrate in cross-sectional representation a preferred embodiment of the present invention.
- FIG. 6 is a cross-sectional representation of the tool that may be used with the present invention.
- FIG. 7A and 7B are top down, plan views of the permissible magnet orientations.
- Unless otherwise specified, all structures, layers, etc. may be formed or accomplished by conventional methods known in the prior art.
- Accordingly as shown in FIG. 1, a conventional aluminum or aluminum alloy metallization typically is comprised of dielectric layer30 (e.g. ILD, IMD, or oxide),
bottom barrier layer 10, bulk aluminum oraluminum alloy 12, andupper barrier layer 14. Patternedphotoresist layer 16 overliesupper barrier layer 14. - Barrier layers10, 14 are preferably comprised of an
inner Ti layer aluminum alloy 12, andouter TiN layer aluminum alloy 12. Barrier layers 10, 14 may also be comprised of other metal or metal alloys such as tantalum, tungsten, molybdenum, chromium, vanadium, niobium, zirconium, or metal-silicon nitrides. - Barrier layers10, 14 are preferably from about 5 to 150 nm thick.
- Bulk aluminum or
aluminum alloy 12 is preferably an aluminum copper alloy with 0.5% copper (Al-0.5% Cu or just Al(Cu)). Al(Cu)layer 12 is preferably from about 100 to 1500 nm thick. -
Photoresist layer 16 may be comprised of a variety of organic materials, such as Barl 900™ material manufactured by Brewer Science, U.S.A., or Novalic material because they are photosensitive. - As shown in FIG. 2, as the metallization is etched by a chlorine -containing plasma, certain byproducts such as aluminum chloride are pumped out of the reaction chamber. However, non-gaseous byproducts, which can include carbon, oxygen, titanium, or other materials will form a thin deposited film/layer/
polymer 20 on thesidewalls 22 oftrench 24 which is formed inregion 18. - These byproducts result from the reactions of
photoresist 16 with the etchants, as well as the etching byproducts formed from barrier layer 14 (TiN layer 14A/Ti layer 14B) - The metallization etch process includes the following parameters: from about 0 to 100 sccm BCl3 gas flow, from about 0 to 200 sccm Cl2 gas flow, from about 0 to 20 sccm N2 gas flow, from about 0 to 20 sccm CH4 gas flow, and from about 0 to 20 sccm CHF3. Either a Lam Research model TCP 9600 tool or an AMAT (Applied Materials) model DPS metal tool may be used.
- As shown in FIG. 3, as the metallization is etched through bottom barrier layer10 (
Ti layer 10B/TiN layer 10A),polymer layer 20 extends to the etched sidewalls ofbarrier layer 10. -
Polymer layer 20 serves to protectsidewalls 22 from the etchant and preserve the anisotropic nature of the etching, i.e. maintenance ofvertical sidewalls 22. - Since the conventional metal stack for aluminum—0.5% copper alloy (Al(Cu)) is
photoresist 16/TiN layer 14A/Ti layer 14B/Al(Cu)layer 12/Ti layer 10B/TiN layer 10A/oxide layer 30, the property of thesidewall polymer 20 that forms over thesidewalls 22 of the etched structure is organic plus oxide-like. Thispolymer 20 is quite a bit stickier on the metal line andsidewall 22 after plasma etching and in-situ photoresist (PR) 16 stripping. A strategy is therefore needed for a dry clean oxide (sidewall polymer 20) andPR 16 removal. - The inventors have discovered that removing the
polymer layer 20 requires the use of a two step process (Step I and Step II): - STEP I. low pressure of less than 50 millitorr, more preferably from about 10 to 50 millitorr, and most preferably about 20 millitorr;
- medium RF power of greater than about 200 W, more preferably from about 200 to 500 W, and most preferably about 300W;
- a magnetic field greater than about 10 gauss (G), more preferably from about 20 to 100 gauss, and most preferably about 20 gauss at a radio frequency of about 13.56 MHz;
- and the use of a fluorine containing gas/oxygen containing gas mixture having a preferable fluorine gas:oxygen gas ratio about 1 to 4; the fluorine containing gas may be CF4, NF3, or CHF3, and is preferably CF4; the oxygen containing gas may be O2, or O3, and is preferably O2.
- at a hardware setting temperature from about 20 to 100° C.;
- for from about 10 to 60 seconds and more preferably from about 28 to 32 seconds, and most preferably about 30 seconds;
- followed by a:
- STEP II. deionized water (DI) rinse step preferably with megasonic power from about 0 to 500W to take away all the debris and PR ash.
- As shown in FIG. 4, initial treatment of the structure of FIG. 3 leaves
sidewall polymer residue 20 extending overouter TiN layer 14A. - As shown in FIG. 5, further treating the structure of FIG. 4 in accordance with the present invention removes the
polymer layer 20 from sidewalls 22 withintrench 24 and fromouter TiN layer 14A. - FIG. 6 illustrates the major elements of the tool that may be used in the present invention. The
wafer 60 is supported by an electrode statistic chuck (ESC) 62 withinprocessing chamber 64.RF power source 66 supplies the necessary RF power. Processingchamber 64 is flanked bymagnetic field 68. - FIGS. 7A and 7B, respectively, illustrate top down, plan views of two
permissible magnet - The following tools/models may also be used in the invention: Lam Research model TCP 9600 tool and the AMAT model DPS-metal tool. The following tool configurations may also be used: magnetic enhanced RIE and magnetic confinement triode RIE.
- The table below illustrates the contrasting parameters for two other dry cleaning process where “Dry Clean (A)” is a GaSonics vendor process, “Dry Clean (B)” is a Ulvac vendor process which each use a downstream microwave power; and the most preferred parameters for the step one of the present invention (“Invention”):
Process Dry Clean (A) Dry Clean (B) Invention Parameter Step 1 Step 2 Step 1Step 2 One Step Platen Temp 30 30 40 30 15 (° C.) Pins Down Down 2 2 — (up/down) Pressure 700 700 450 350 20 (millitorr) Microwave 1400 — 1500 — — Power RF/Platen — 200 150 225 300 Power O2 (sccm) 800 — 980 — 40 N2/H2 (sccm) — 500 100 480 — NF3 (sccm) — — 80 — — CF4 200 50 — 20 10 Magnetic (G) — — — — 20 Step Time 30 30 30 20 30 (sec) - The significant parameters in the above table are in bold. Low pressure—most preferably 20 mT versus 350 to 700 mT in the prior processes; no microwave power versus 1400 to 1500 in the prior processes; and a magnetic field of most preferably 20 gauss versus no magnetic field in the prior processes, used in the dry cleaning method of the present invention admirably removes
polymer layer 22 from withintrench 24 versus the prior dry clean processes and without the attendant problems of metal corrosion and metal pitting, for example, common to prior wet cleaning processes. - It is believed that the use of a magnetic field with a low pressure without a downstream microwave power is an important feature of the invention as it can improve plasma density and increase ion acceleration.
- Further advantages of the present invention include:
- metal corrosion and metal pitting are prevented;
- the defect density of the devices are lowered;
- the time required to repair defects is minimized and so the product cycle time is lowered;
- the yield is increased due to the decreased defect density;
- elimination of wet chemicals reduces the cost of purchasing, handling and properly disposing such chemicals; and
- no wet chemicals eliminates a source of electrolytes and so eliminates any deleterious electrogalavanic processes.
- In processes known to the inventors, fluorine gas is useful for oxide removal (such as TiOx, AlOx, CuOx, and SiO2), and an O2/N2 gas mixture or an H2/N2 gas mixture or both gas mixtures is useful for
photoresist layer 16 removal/strip. So it would be anticipated that using fluorine gas with an O2/N2 gas mixture or an H2/N2 gas mixture or both gas mixtures would be useful to stripphotoresist layer 16 and to removesidewall polymer layer 20. - However, attempts made using microwave power and the above combination gas mixture does not remove
sidewall polymer layer 20 well. Further, attempts made to introduce the bottom power (bias RF power) also failed to effectively removesidewall polymer layer 20. - While particular embodiments of the present invention have been illustrated and described, it is not intended to limit the invention, except as defined by the following claims.
Claims (23)
1. A dry cleaning method for use in semiconductor fabrication, including the steps of:
providing an etched metallization structure;
placing said etched metallization structure in a processing chamber; and
cleaning said etched metallization structure by introducing a fluorine containing gas/oxygen containing gas mixture into said processing chamber proximate said etched metallization structure without the use of a downstream microwave while applying a magnetic field proximate said etched metallization structure and maintaining a pressure of less than about 50 millitorr within said processing chamber for a predetermined time.
2. The method of claim 1 , further including the step of then rinsing said etched metallization structure with deionized water.
3. The method of claim 1 , further including the step of rinsing said etched metallization structure with deionized water at a megasonic power from about 0 to 500W.
4. The method of claim 1 , wherein said etched metallization structure includes an upper barrier layer, bulk Al-0.5% Cu alloy, and a bottom barrier layer.
5. The method of claim 1 , wherein said fluorine containing gas/oxygen containing gas mixture has a fluorine containing gas:oxygen containing gas ratio of about 1:4; said magnetic field is greater than about 10 gauss; said pressure is from about 10 to 50 millitorr, and said predetermined time is from about 28 to 32 seconds.
6. The method of claim 1 , wherein said fluorine containing gas/oxygen containing gas mixture has a fluorine containing gas:oxygen containing gas ratio of about 1:4; said magnetic field is from about 20 to 100 gauss; said pressure is about 20 millitorr, and said predetermined time is about 30 seconds.
7. The method of claim 1 , wherein said cleaning step includes maintaining an RF power of greater than about 200 W; said magnetic field is from about 20 to 100 gauss at a radio frequency of about 13.56 MHz; and said predetermined time is from about 10 to 60 seconds.
8. The method of claim 1 , wherein said cleaning step includes maintaining an RF power of from about 200 to 500 W; said magnetic field is from about 20 to 100 gauss at a radio frequency of about 13.56 MHz; and said predetermined time is from about 28 to 32 seconds.
9. The method of claim 1 , wherein said cleaning step includes maintaining an RF power of about 300 W; said magnetic field is about 20 gauss at a radio frequency of about 13.56 MHz; and said predetermined time is about 30 seconds.
10. A dry cleaning method for use in semiconductor fabrication, including the steps of:
providing an etched metallization structure;
placing said etched metallization structure in a processing chamber;
cleaning said etched metallization structure by introducing a fluorine containing gas/oxygen containing gas mixture into said processing chamber proximate said etched metallization structure without the use of a downstream microwave while applying a magnetic field proximate said etched metallization structure and maintaining a pressure of less than about 50 millitorr within said processing chamber for a predetermined time; and
rinsing said etched metallization structure with deionized water.
11. The method of claim 10 , wherein said deionized water rinsing step is conducted at a megasonic power from about 250 to 350.
12. The method of claim 10 , wherein said etched metallization structure includes an upper barrier layer, bulk Al-0.5% Cu alloy, and a bottom barrier layer.
13. The method of claim 10 , wherein said fluorine containing gas/oxygen containing gas mixture has a fluorine containing gas:oxygen containing gas ratio of about 1:4; said magnetic field is greater than about 10 gauss; said pressure is from about 10 to 50 millitorr, and said predetermined time is from about 28 to 32 seconds.
14. The method of claim 10 , wherein said fluorine containing gas/oxygen containing gas mixture has a fluorine containing gas:oxygen containing gas ratio of about 1:4; said magnetic field is from about 20 to 100 gauss; said pressure is about 20 millitorr, and said predetermined time is about 30 seconds.
15. The method of claim 10 , wherein said cleaning step includes maintaining an RF power of greater than about 200 W; said magnetic field is greater than about 10 gauss at a radio frequency of about 13.56 MHz; and said predetermined time is from about 10 to 60 seconds.
16. The method of claim 10 , wherein said cleaning step includes maintaining an RF power of from about 200 to 500 W; said magnetic field is from about 20 to 100 gauss at a radio frequency of about 13.56 MHz; and said predetermined time is from about 28 to 32 seconds.
17. The method of claim 10 , wherein said cleaning step includes maintaining an RF power of about 300 W; said magnetic field is about 20 gauss at a radio frequency of about 13.56 MHz; and said predetermined time is about 30 seconds.
18. A dry cleaning method for use in semiconductor fabrication, including the steps of:
providing an aluminum alloy layer over a substrate and a resist layer over said aluminum alloy layer;
reactive ion etching said aluminum alloy layer using a Cl-containing plasma to form a patterned aluminum alloy layer with a polymer on a sidewall of said patterned aluminum alloy layer;
placing said substrate in a processing chamber; and
removing said resist and said polymer and cleaning said patterned aluminum alloy layer by introducing a fluorine containing gas/oxygen containing gas mixture into said processing chamber proximate said etched metallization structure without the use of a downstream microwave while applying a magnetic field of greater than about 10 gauss at a radio frequency of about 13.56 MHz proximate said etched metallization structure at an RF power greater than about 200 W, and maintaining a pressure of less than about 50 millitorr within said processing chamber for from about 28 to 32 seconds.
19. The method of claim 18 , wherein said deionized water rinsing step is conducted at a megasonic power from about 250 to 350.
20. The method of claim 18 , wherein said patterned aluminum alloy layer includes an upper barrier layer, bulk Al-0.5% Cu alloy, and a bottom barrier layer.
21. The method of claim 18 , wherein said fluorine containing gas/oxygen containing gas mixture has a fluorine containing gas:oxygen containing gas ratio of about 1:4; said magnetic field is from about 20 to 100 gauss at a radio frequency of about 13.56 MHz; said RF power is from about 200 to 500 W, said pressure is from about 10 to 50 millitorr, and said predetermined time is from about 28 to 32 seconds.
22. The method of claim 18 , wherein said fluorine containing gas/oxygen containing gas mixture has a fluorine containing gas:oxygen containing gas ratio of about 1:4; said magnetic field is about 20 gauss at a radio frequency of about 13.56 MHz; said RF power is about 300 W, said pressure is about 20 millitorr, and said predetermined time is about 30 seconds.
23. The method of claim 18 including the step of rinsing said patterned aluminum alloy layer with deionized water with a megasonic power from about 250 to 350 W.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060108323A1 (en) * | 2003-06-30 | 2006-05-25 | Shuichi Okawa | Dry etching method |
US20120021538A1 (en) * | 2010-07-26 | 2012-01-26 | Tokyo Electron Limited | Plasma processing method and storage medium |
WO2018052494A1 (en) * | 2016-09-14 | 2018-03-22 | Mattson Technology, Inc. | Strip process for high aspect ratio structure |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002158213A (en) * | 2000-11-21 | 2002-05-31 | Sharp Corp | Method of manufacturing semiconductor device |
US6796314B1 (en) * | 2001-09-07 | 2004-09-28 | Novellus Systems, Inc. | Using hydrogen gas in a post-etch radio frequency-plasma contact cleaning process |
JP4053320B2 (en) * | 2002-03-18 | 2008-02-27 | 沖電気工業株式会社 | Electrode forming method for surface acoustic wave device |
US7456476B2 (en) | 2003-06-27 | 2008-11-25 | Intel Corporation | Nonplanar semiconductor device with partially or fully wrapped around gate electrode and methods of fabrication |
US6909151B2 (en) * | 2003-06-27 | 2005-06-21 | Intel Corporation | Nonplanar device with stress incorporation layer and method of fabrication |
US7268058B2 (en) * | 2004-01-16 | 2007-09-11 | Intel Corporation | Tri-gate transistors and methods to fabricate same |
US7154118B2 (en) * | 2004-03-31 | 2006-12-26 | Intel Corporation | Bulk non-planar transistor having strained enhanced mobility and methods of fabrication |
US7579280B2 (en) * | 2004-06-01 | 2009-08-25 | Intel Corporation | Method of patterning a film |
US20050279453A1 (en) * | 2004-06-17 | 2005-12-22 | Uvtech Systems, Inc. | System and methods for surface cleaning |
US7042009B2 (en) | 2004-06-30 | 2006-05-09 | Intel Corporation | High mobility tri-gate devices and methods of fabrication |
US7348284B2 (en) | 2004-08-10 | 2008-03-25 | Intel Corporation | Non-planar pMOS structure with a strained channel region and an integrated strained CMOS flow |
US7332439B2 (en) * | 2004-09-29 | 2008-02-19 | Intel Corporation | Metal gate transistors with epitaxial source and drain regions |
US7422946B2 (en) * | 2004-09-29 | 2008-09-09 | Intel Corporation | Independently accessed double-gate and tri-gate transistors in same process flow |
US7361958B2 (en) * | 2004-09-30 | 2008-04-22 | Intel Corporation | Nonplanar transistors with metal gate electrodes |
US20060086977A1 (en) | 2004-10-25 | 2006-04-27 | Uday Shah | Nonplanar device with thinned lower body portion and method of fabrication |
US7518196B2 (en) | 2005-02-23 | 2009-04-14 | Intel Corporation | Field effect transistor with narrow bandgap source and drain regions and method of fabrication |
US20060202266A1 (en) * | 2005-03-14 | 2006-09-14 | Marko Radosavljevic | Field effect transistor with metal source/drain regions |
US7858481B2 (en) | 2005-06-15 | 2010-12-28 | Intel Corporation | Method for fabricating transistor with thinned channel |
US7547637B2 (en) | 2005-06-21 | 2009-06-16 | Intel Corporation | Methods for patterning a semiconductor film |
US7279375B2 (en) * | 2005-06-30 | 2007-10-09 | Intel Corporation | Block contact architectures for nanoscale channel transistors |
US7402875B2 (en) * | 2005-08-17 | 2008-07-22 | Intel Corporation | Lateral undercut of metal gate in SOI device |
US8481142B1 (en) * | 2005-08-30 | 2013-07-09 | National Semiconductor Corporation | System and method for monitoring chloride content and concentration induced by a metal etch process |
US20070090416A1 (en) | 2005-09-28 | 2007-04-26 | Doyle Brian S | CMOS devices with a single work function gate electrode and method of fabrication |
US7479421B2 (en) | 2005-09-28 | 2009-01-20 | Intel Corporation | Process for integrating planar and non-planar CMOS transistors on a bulk substrate and article made thereby |
US20070090408A1 (en) * | 2005-09-29 | 2007-04-26 | Amlan Majumdar | Narrow-body multiple-gate FET with dominant body transistor for high performance |
US7485503B2 (en) | 2005-11-30 | 2009-02-03 | Intel Corporation | Dielectric interface for group III-V semiconductor device |
US20070152266A1 (en) * | 2005-12-29 | 2007-07-05 | Intel Corporation | Method and structure for reducing the external resistance of a three-dimensional transistor through use of epitaxial layers |
KR101226667B1 (en) * | 2006-01-12 | 2013-01-25 | 삼성디스플레이 주식회사 | Method for manufacturing metal line and display substrate having the metal line |
US8143646B2 (en) | 2006-08-02 | 2012-03-27 | Intel Corporation | Stacking fault and twin blocking barrier for integrating III-V on Si |
US20080157225A1 (en) * | 2006-12-29 | 2008-07-03 | Suman Datta | SRAM and logic transistors with variable height multi-gate transistor architecture |
US8362566B2 (en) | 2008-06-23 | 2013-01-29 | Intel Corporation | Stress in trigate devices using complimentary gate fill materials |
WO2011008436A2 (en) * | 2009-07-13 | 2011-01-20 | Applied Materials, Inc. | Method for removing implanted photo resist from hard disk drive substrates |
US8673162B2 (en) * | 2009-12-10 | 2014-03-18 | Applied Materials, Inc. | Methods for substrate surface planarization during magnetic patterning by plasma immersion ion implantation |
JP6227396B2 (en) * | 2013-12-20 | 2017-11-08 | 株式会社ジャパンディスプレイ | THIN FILM TRANSISTOR AND DISPLAY DEVICE USING THE SAME |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5578161A (en) * | 1991-04-30 | 1996-11-26 | International Business Machines Corporation | Method and apparatus for in-situ and on-line monitoring of trench formation process |
US5667630A (en) * | 1995-04-28 | 1997-09-16 | Vanguard International Semiconductor Corporation | Low charge-up reactive ion metal etch process |
US5906948A (en) * | 1998-04-17 | 1999-05-25 | Vanguard International Semiconductor Corporation | Method for etching high aspect-ratio multilevel contacts |
US6146542A (en) * | 1998-01-09 | 2000-11-14 | Hyundia Electronics Industries Co., Ltd. | Dry etching method of multilayer film |
US6303513B1 (en) * | 1999-06-07 | 2001-10-16 | Applied Materials, Inc. | Method for controlling a profile of a structure formed on a substrate |
US6358670B1 (en) * | 1999-12-28 | 2002-03-19 | Electron Vision Corporation | Enhancement of photoresist plasma etch resistance via electron beam surface cure |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4501061A (en) | 1983-05-31 | 1985-02-26 | Advanced Micro Devices, Inc. | Fluorine plasma oxidation of residual sulfur species |
JPH07109825B2 (en) | 1992-01-13 | 1995-11-22 | 富士通株式会社 | Dry cleaning method for semiconductor substrate surface or thin film surface |
JPH05291201A (en) | 1992-04-08 | 1993-11-05 | Sony Corp | Formation method for aluminum-based pattern |
US5599743A (en) | 1994-04-07 | 1997-02-04 | Matsushita Electronics Corporation | Method of manufacturing a semiconductor device |
JP3247270B2 (en) | 1994-08-25 | 2002-01-15 | 東京エレクトロン株式会社 | Processing apparatus and dry cleaning method |
US5908319A (en) | 1996-04-24 | 1999-06-01 | Ulvac Technologies, Inc. | Cleaning and stripping of photoresist from surfaces of semiconductor wafers |
US5882489A (en) | 1996-04-26 | 1999-03-16 | Ulvac Technologies, Inc. | Processes for cleaning and stripping photoresist from surfaces of semiconductor wafers |
US5976986A (en) | 1996-08-06 | 1999-11-02 | International Business Machines Corp. | Low pressure and low power C12 /HC1 process for sub-micron metal etching |
US5795831A (en) | 1996-10-16 | 1998-08-18 | Ulvac Technologies, Inc. | Cold processes for cleaning and stripping photoresist from surfaces of semiconductor wafers |
US5849639A (en) * | 1997-11-26 | 1998-12-15 | Lucent Technologies Inc. | Method for removing etching residues and contaminants |
US6017826A (en) | 1998-10-05 | 2000-01-25 | Chartered Semiconductor Manufacturing, Ltd. | Chlorine containing plasma etch method with enhanced sidewall passivation and attenuated microloading effect |
US6379574B1 (en) * | 1999-05-03 | 2002-04-30 | Applied Materials, Inc. | Integrated post-etch treatment for a dielectric etch process |
-
2000
- 2000-06-12 US US09/591,848 patent/US6526996B1/en not_active Expired - Lifetime
-
2003
- 2003-01-09 US US10/339,157 patent/US20030104697A1/en not_active Abandoned
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5578161A (en) * | 1991-04-30 | 1996-11-26 | International Business Machines Corporation | Method and apparatus for in-situ and on-line monitoring of trench formation process |
US5667630A (en) * | 1995-04-28 | 1997-09-16 | Vanguard International Semiconductor Corporation | Low charge-up reactive ion metal etch process |
US6146542A (en) * | 1998-01-09 | 2000-11-14 | Hyundia Electronics Industries Co., Ltd. | Dry etching method of multilayer film |
US5906948A (en) * | 1998-04-17 | 1999-05-25 | Vanguard International Semiconductor Corporation | Method for etching high aspect-ratio multilevel contacts |
US6303513B1 (en) * | 1999-06-07 | 2001-10-16 | Applied Materials, Inc. | Method for controlling a profile of a structure formed on a substrate |
US6358670B1 (en) * | 1999-12-28 | 2002-03-19 | Electron Vision Corporation | Enhancement of photoresist plasma etch resistance via electron beam surface cure |
Cited By (13)
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US20060108323A1 (en) * | 2003-06-30 | 2006-05-25 | Shuichi Okawa | Dry etching method |
US7727412B2 (en) * | 2003-06-30 | 2010-06-01 | Tdk Corporation | Dry etching method |
US20120021538A1 (en) * | 2010-07-26 | 2012-01-26 | Tokyo Electron Limited | Plasma processing method and storage medium |
CN102347231A (en) * | 2010-07-26 | 2012-02-08 | 东京毅力科创株式会社 | Plasma processing method and plasma processing apparatus |
US8404590B2 (en) * | 2010-07-26 | 2013-03-26 | Tokyo Electron Limited | Plasma processing method and storage medium |
WO2018052494A1 (en) * | 2016-09-14 | 2018-03-22 | Mattson Technology, Inc. | Strip process for high aspect ratio structure |
CN109690735A (en) * | 2016-09-14 | 2019-04-26 | 马特森技术有限公司 | Stripping means for high-aspect-ratio structure |
KR20190043556A (en) * | 2016-09-14 | 2019-04-26 | 맷슨 테크놀로지, 인크. | Strip process with high aspect ratio structure |
JP2019530230A (en) * | 2016-09-14 | 2019-10-17 | マットソン テクノロジー インコーポレイテッドMattson Technology, Inc. | Strip process for high aspect ratio structures |
US10599039B2 (en) | 2016-09-14 | 2020-03-24 | Mattson Technology, Inc. | Strip process for high aspect ratio structure |
KR102204116B1 (en) | 2016-09-14 | 2021-01-19 | 베이징 이타운 세미컨덕터 테크놀로지 컴퍼니 리미티드 | Strip process with high aspect ratio structures |
US10901321B2 (en) | 2016-09-14 | 2021-01-26 | Mattson Technology, Inc. | Strip process for high aspect ratio structure |
TWI760338B (en) * | 2016-09-14 | 2022-04-11 | 美商得昇科技股份有限公司 | Strip process for high aspect ratio structure |
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