US20010003271A1 - Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film - Google Patents
Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film Download PDFInfo
- Publication number
- US20010003271A1 US20010003271A1 US09/731,722 US73172200A US2001003271A1 US 20010003271 A1 US20010003271 A1 US 20010003271A1 US 73172200 A US73172200 A US 73172200A US 2001003271 A1 US2001003271 A1 US 2001003271A1
- Authority
- US
- United States
- Prior art keywords
- gas
- chamber
- film
- processing apparatus
- substrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000012545 processing Methods 0.000 title claims abstract description 51
- 238000005260 corrosion Methods 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 claims abstract description 51
- 230000008569 process Effects 0.000 claims abstract description 46
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 42
- 229910052593 corundum Inorganic materials 0.000 claims abstract description 40
- 229910001845 yogo sapphire Inorganic materials 0.000 claims abstract description 40
- 239000000758 substrate Substances 0.000 claims abstract description 29
- 238000010438 heat treatment Methods 0.000 claims abstract description 9
- 239000007789 gas Substances 0.000 claims description 227
- 239000000463 material Substances 0.000 claims description 21
- 230000007797 corrosion Effects 0.000 claims description 19
- 238000005530 etching Methods 0.000 claims description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 16
- 239000002826 coolant Substances 0.000 claims description 9
- 239000000919 ceramic Substances 0.000 claims description 7
- 230000005672 electromagnetic field Effects 0.000 claims description 7
- 230000007246 mechanism Effects 0.000 claims description 7
- 238000004380 ashing Methods 0.000 claims description 6
- 229910052681 coesite Inorganic materials 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 229910052906 cristobalite Inorganic materials 0.000 claims description 6
- 230000000737 periodic effect Effects 0.000 claims description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- 229910052682 stishovite Inorganic materials 0.000 claims description 6
- 229910052905 tridymite Inorganic materials 0.000 claims description 6
- 229910017083 AlN Inorganic materials 0.000 claims description 5
- 229910045601 alloy Inorganic materials 0.000 claims description 5
- 239000000956 alloy Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- -1 Sc2F3 Inorganic materials 0.000 claims description 3
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims description 3
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims description 3
- RSEIMSPAXMNYFJ-UHFFFAOYSA-N europium(III) oxide Inorganic materials O=[Eu]O[Eu]=O RSEIMSPAXMNYFJ-UHFFFAOYSA-N 0.000 claims description 3
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum oxide Inorganic materials [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- KTUFCUMIWABKDW-UHFFFAOYSA-N oxo(oxolanthaniooxy)lanthanum Chemical compound O=[La]O[La]=O KTUFCUMIWABKDW-UHFFFAOYSA-N 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- HYXGAEYDKFCVMU-UHFFFAOYSA-N scandium(III) oxide Inorganic materials O=[Sc]O[Sc]=O HYXGAEYDKFCVMU-UHFFFAOYSA-N 0.000 claims description 3
- 230000006698 induction Effects 0.000 claims 6
- 229910009527 YF3 Inorganic materials 0.000 claims 2
- 230000003247 decreasing effect Effects 0.000 claims 1
- 239000004065 semiconductor Substances 0.000 abstract description 6
- 239000010408 film Substances 0.000 description 101
- 229910020323 ClF3 Inorganic materials 0.000 description 27
- JOHWNGGYGAVMGU-UHFFFAOYSA-N trifluorochlorine Chemical compound FCl(F)F JOHWNGGYGAVMGU-UHFFFAOYSA-N 0.000 description 27
- 229910003074 TiCl4 Inorganic materials 0.000 description 26
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 26
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 24
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 22
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 18
- 230000015572 biosynthetic process Effects 0.000 description 14
- 238000004140 cleaning Methods 0.000 description 13
- 229910052782 aluminium Inorganic materials 0.000 description 12
- 239000010410 layer Substances 0.000 description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 238000005229 chemical vapour deposition Methods 0.000 description 10
- 230000004888 barrier function Effects 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- 229910019901 yttrium aluminum garnet Inorganic materials 0.000 description 7
- JNDMLEXHDPKVFC-UHFFFAOYSA-N aluminum;oxygen(2-);yttrium(3+) Chemical compound [O-2].[O-2].[O-2].[Al+3].[Y+3] JNDMLEXHDPKVFC-UHFFFAOYSA-N 0.000 description 6
- 239000002131 composite material Substances 0.000 description 6
- 238000009792 diffusion process Methods 0.000 description 6
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- 238000002441 X-ray diffraction Methods 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000010409 thin film Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 239000003990 capacitor Substances 0.000 description 4
- 230000001939 inductive effect Effects 0.000 description 4
- 238000009616 inductively coupled plasma Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- HDZGCSFEDULWCS-UHFFFAOYSA-N monomethylhydrazine Chemical compound CNN HDZGCSFEDULWCS-UHFFFAOYSA-N 0.000 description 4
- PBCFLUZVCVVTBY-UHFFFAOYSA-N tantalum pentoxide Inorganic materials O=[Ta](=O)O[Ta](=O)=O PBCFLUZVCVVTBY-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 230000010354 integration Effects 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 230000002093 peripheral effect Effects 0.000 description 3
- 238000005240 physical vapour deposition Methods 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000010420 art technique Methods 0.000 description 2
- 230000002238 attenuated effect Effects 0.000 description 2
- 229910010293 ceramic material Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000002230 thermal chemical vapour deposition Methods 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
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910052692 Dysprosium Inorganic materials 0.000 description 1
- 229910052693 Europium Inorganic materials 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 229910020177 SiOF Inorganic materials 0.000 description 1
- 229910008482 TiSiN Inorganic materials 0.000 description 1
- 229910001080 W alloy Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- SWUWMVIPFQAITJ-UHFFFAOYSA-N chlorine difluoride-35cl Chemical compound FClF SWUWMVIPFQAITJ-UHFFFAOYSA-N 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000001020 plasma etching Methods 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052706 scandium Inorganic materials 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45563—Gas nozzles
- C23C16/45565—Shower nozzles
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/4401—Means for minimising impurities, e.g. dust, moisture or residual gas, in the reaction chamber
- C23C16/4404—Coatings or surface treatment on the inside of the reaction chamber or on parts thereof
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45514—Mixing in close vicinity to the substrate
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45561—Gas plumbing upstream of the reaction chamber
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45563—Gas nozzles
- C23C16/45574—Nozzles for more than one gas
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45563—Gas nozzles
- C23C16/4558—Perforated rings
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/50—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges
- C23C16/505—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges using radio frequency discharges
- C23C16/507—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges using radio frequency discharges using external electrodes, e.g. in tunnel type reactors
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/10—Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
- C23C4/11—Oxides
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32009—Arrangements for generation of plasma specially adapted for examination or treatment of objects, e.g. plasma sources
- H01J37/32082—Radio frequency generated discharge
- H01J37/321—Radio frequency generated discharge the radio frequency energy being inductively coupled to the plasma
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32431—Constructional details of the reactor
- H01J37/32458—Vessel
- H01J37/32477—Vessel characterised by the means for protecting vessels or internal parts, e.g. coatings
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32431—Constructional details of the reactor
- H01J37/32458—Vessel
- H01J37/32477—Vessel characterised by the means for protecting vessels or internal parts, e.g. coatings
- H01J37/32495—Means for protecting the vessel against plasma
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- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
Definitions
- a present invention relates to a processing chamber having a mounted chamber having a high-corrosion-resistant film and applied to a film forming apparatus, heat processing apparatus and etching apparatus as used in a CVD (Chemical Vapor Deposition), etc.
- CVD Chemical Vapor Deposition
- a barrier layer is formed on the bottom and inner wall of the hole before forming a buried layer in the contact hole or via hole and then such a buried layer is formed.
- a TiN film is known as a barrier layer.
- a high dielectric constant material such as Ta 2 O 5 is used as a capacitor gate material to obtain a higher capacitance without changing its scale.
- a higher dielectric constant material is not stabler in characteristic than SiO 2 conventionally used as the capacitor gate material. If a poly-Si is used on the overlying electrode, it is oxidized due to the chemical reaction after the formation of the capacitance, thus failing to manufacture a device element of stable characteristics. It is, therefore, necessary that a less-oxidized TiN film be used as an overlying electrode.
- the TiN film has been formed by using a physical vapor deposition (PVD) technique and a demand has been made for a finer and higher integration device in particular.
- PVD physical vapor deposition
- the design rules are particularly stringent.
- CVD chemical vapor deposition
- a thermal CVD is used, in which TiCl 4 and NH 3 (ammonia) or MMH (monomethylhydrazine) is applied, as a reaction gas, to a heated substrate.
- the TiN film being a columnar crystal, is liable to be boundary-diffused and involves a lower barrier characteristic.
- the lower barrier characteristic presents a problem in the case where the TiN film is used as a barrier layer for a Cu connection line or an oxygen diffusion barrier for Ta 2 O 5 connection line of an electrode overlying the capacitor. That is, a problem occurs due to the corrosion of the Cu connection line by the residual chlorine or a lowering of a capacitance of Ta 2 O 5 by the diffusion of oxygen.
- An amount of Cl in the formed film can be indeed reduced by making a film formation temperature higher.
- a high temperature process is not preferable due to a problem, such as thermal resistance and the corrosion, of a connection line material such as Cu and Al.
- ICP Inductively Coupled Plasma
- an antenna member such as a coil is provided around a bell jar (chamber).
- an inductive electromagnetic field is created to provide plasma.
- the TiN film becomes low-resistance and low in chlorine, and even a film formed at a relatively low temperature is made low in an amount of residual chlorine.
- a deposit is formed on the inner wall of the chamber due to the introduction of a process gas from above the chamber and a foreign deposit is liable to be formed.
- the plasma created is attenuated due to the deposit of a conductive film on the inner wall of the upper chamber, thus making it difficult to form a film.
- An object of the present invention is to provide a processing apparatus having a chamber applied to a film forming apparatus, heat processing apparatus and etching apparatus and having a high-corrosion-resistant property and less liable to deposit a product by a process gas or a product, such as an etching product, on its inner wall thereof.
- the thus constructed processing apparatus has a mounted chamber holding a to-be-processed substrate and having members for work-processing the substrate by any of heating, plasma, process gas or a combination thereof, in which a film of Al 2 O 3 and Y 2 O 3 is formed on the inner wall surface of the chamber and on the exposed surfaces of the members within the chamber, the Al 2 O 3 /Y 2 O 3 weight ratio being above 0.5.
- the Al 2 O 3 /Y 2 O 3 weight ratio is in a range above 0.5 but below 4.
- the thickness of the formed film is above 50 ⁇ m.
- FIG. 1 is a view showing a practical structure of a plasma CVD apparatus according to a first embodiment of the present invention
- FIGS. 2A and 2B are views showing a sample of a test by etching and evaluation standard
- FIG. 3 is a view showing a relation of members in an etching time to an etched amount
- FIG. 7 is a view showing a rate of a composite oxide when the Al 2 O 3 /Y 2 O 3 weight ratio of a sprayed film varies;
- FIG. 8 is a view showing a relation of an Al 2 O 3 /Y 2 O 3 weight ratio of a sprayed film to an etched amount
- FIG. 9 is a view showing an X-ray diffraction pattern of a sprayed film when sprayed is made using a YAG;
- FIG. 10 is a view showing a practical form of a plasma CVD apparatus according to a second embodiment
- FIG. 11 is a view showing a practical form of a plasma CVD apparatus according to a third embodiment
- FIG. 12 is a view showing a practical structure of a plasma CVD apparatus according to a fourth embodiment
- FIGS. 13A and 13B show a practical structure of a shower head in the fourth embodiment
- FIGS. 14A and 14B are a view showing a modified structure of the shower head in the fourth embodiment
- FIG. 15 is a view showing practical structures of head section
- FIG. 16 is a perspective view showing a first modified structure of a gas discharge member
- FIG. 17 is a perspective view showing a second modified structure of a gas discharge member
- FIG. 18 is a view showing one form of a lower-height thin type chamber
- FIG. 19 is a view showing one form of a semi-spherical type chamber
- FIG. 20 is a view showing one form of a dome-type chamber
- FIG. 21 is a view showing a practical structure of a heat processing apparatus
- FIG. 22 is a view showing a practical structure of an ashing apparatus
- FIG. 23 is a view showing a practical structure of an etching apparatus.
- FIG. 24 is a view showing a relation of a breakdown voltage to the thickness of the sprayed film in the respective embodiment of the present invention.
- FIG. 1 is a cross-sectional view showing a practical example applied to a CVD film forming apparatus as a first embodiment of the present invention in a processing apparatus having a mounted chamber having a high corrosion-resistant thermal sprayed film.
- the film forming apparatus of the present invention is directed to forming, for example, a TiN thin film.
- the film forming apparatus 10 includes a chamber 11 having a lower chamber 11 a and upper chamber 11 formed as an integral unit in a hermetically sealable way.
- the upper chamber 11 b is made smaller in diameter than the lower chamber 11 a .
- the lower chamber 11 a is comprised of an electric conductor 12 , such as aluminum, whose surface is anadigation processed for example.
- the upper chamber 11 b comprises a base material 13 of, for example, a ceramic material and a sprayed film 14 .
- the film 14 may contain oxide of Y, Sc, La, Ce, Eu, Dy or the like, or fluoride of one of these metals.
- the film 14 may be made of a compound of a III-a element of the periodic table, such as Y 2 O 3 . Needless to say, the film 14 may be made of such a compound and any other material.
- the film 14 containing a compound of a III-a element is a sprayed film that substantially comprises Al2O3 and Y 2 O 3 .
- the material of the chamber use can be made of ceramic (Al 2 O 3 , SiO 2 , AlN etc.,), aluminum or stainless steel, metal or metal alloy.
- a weight ratio of Al 2 O 3 /Y 2 O 3 of the sprayed film 14 is preferably 0.5 to 4. It is to be noted that FIG. 8 simply shows data of the weight ratio of up to 1.5.
- the sprayed film 14 it may be possible to spray an Al 2 O 3 and Y 2 O 3 compound or to spray, for example, yttrium-aluminum-garnet (YAG) in a composite oxide state of the above-mentioned composition range.
- the thickness of the sprayed film is based on the insulation withstand characteristic for plasma generation and, from the standpoint of the breakdown voltage characteristic shown in, for example, FIG. 2, may be of the order of at least 50 ⁇ m and preferably of the order of 50 ⁇ m but not above 300 ⁇ m from the standpoint of a manufacturing process and cost.
- the ceramics of the base material 13 may be Al 2 O 3 , SiO 2 , such as silica glass and quartz, AlN, alternatively, rigid plastic may be used, and, here, the sprayed film as set out above is not formed on the inner wall of the upper chamber 11 b but it may be formed there.
- an insulating plate 15 of ceramic, etc., and support base 16 are provided and a substantially cylindrical susceptor 17 is provided on the support base 16 to place a semiconductor wafer (hereinafter referred to as a wafer) as a to-be-processed object on it.
- a wafer semiconductor wafer
- a coolant chamber 18 is provided in the interior of the support base 16 to receive the coolant via a coolant introducing tube 19 .
- the coolant is discharged out of a discharge tube 20 .
- a cold is conducted through the susceptor 17 to the wafer W.
- a heating element 21 is buried in the susceptor 17 to heat the wafer W to a predetermined temperature by supplying power from a power source 22 .
- a controller 23 is connected to the power source 22 . And the temperature of the wafer W is controlled by a cold of the coolant and heat of the heating element.
- an electrostatic chuck 24 is provided which is substantially the same in configuration as the wafer W.
- the electrostatic chuck 24 is so formed as to have an electrode 26 buried in an insulating material 25 .
- the wafer W is electrostatically attracted by a Coulomb force, etc., generated by applying a DC voltage from a DC power source 27 to the electrode 26 .
- a focusing ring 28 is provided at the outer peripheral portion of an upper surface of the electrostatic chuck 24 to surround the wafer W.
- the above-mentioned sprayed film 14 is formed on those exposed surfaces of the support base 16 , susceptor 17 , electrostatic chuck 24 and focusing ring 28 within the chamber.
- a shower head member 30 is provided above the chamber 11 b .
- many gas discharge holes 30 a (Ar, ClF 3 ), 30 b (Ar, TiCl 4 ) and 30 c (NH 3 ) are alternately formed to discharge gases in a down direction within the chamber.
- the pipes of a gas supply system 40 are connected to the shower head member 30 .
- a pipe 55 for supplying a gas (Ar, ClF 3 ) is connected to the gas discharge holes 30 a
- a pipe 56 for supplying a gas (Ar, TiCl 4 ) is connected to the gas discharge holes 30 b
- a pipe 57 for supplying a gas (NH 3 ) is connected to the gas discharge holes 30 c .
- the shower head member 30 is comprised of, for example, a three-layers-stacked structure of three gas dispersion plate and has discharge plate having the gas discharge holes.
- the respective gas discharge plate has a groove and holes for allowing one kind of gas to be dispersed evenness to a whole gas discharge surface area in the head.
- the discharge holes of the gas dispersion plate are so formed as not be overlapped with the discharge holes of the other gas dispersion plate.
- the gas discharge holes are arranged in a matrix array upon viewing the gas discharge hole surface side from below. And a post-mixing system is adopted according to which TiCl 4 gas and NH 3 gas are discharged from the alternately formed different discharge holes and these gases are mixed as a process gas after being discharged.
- the gas supply system 40 has a ClF 3 supply source 41 for supplying ClF 3 as a cleaning gas, Ar supply sources 42 and 43 for supplying Ar, a TiCl 4 supply source 44 for supplying TiCl 4 as a process gas and an NH 3 supply source 45 for supplying NH 3 as a process gas.
- a gas line 46 is connected to the ClF 3 supply source 41
- gas lines 47 and 48 are connected to the Ar supply sources 42 and 43 , respectively
- a gas line 49 is connected to the TiCl 4 supply source 44 and a gas line 50 is connected to the NH 3 supply source 45 .
- a valve 51 ( 51 a , 51 b ) and mass flow controller 52 are provided at these gas lines.
- the gas line 46 extending from the ClF 3 supply source 41 is joined and the gas line 46 extending form the ClF 3 supply source 41 is joined.
- the gas line 46 extending form the ClF 3 supply source 41 is joined into a gas line 53 .
- ClF 3 serving as a cleaning gas is passed through the gas line 46 and pipe 53 and reaches the shower head 30 to allow it to be introduced via the gas discharge holes 30 a into the upper chamber 11 b .
- Ar alone is supplied from the Ar supply source 42 .
- the gas line 49 extending from the TiCl 4 supply source 44 is joined.
- TiCl 4 gas passed through the gas line 49 and pipe 54 is carried by the argon gas and reaches the shower head 30 .
- the TiCl 4 gas is introduced from the gas discharge holes 30 b into the chamber 11 .
- the NH 3 gas is supplied from the NH 3 supply source 45 past the gas line 50 and pipe 55 to the shower head 30 and introduced from the gas discharge holes 30 c into the upper chamber 11 b .
- monomethylhydrazine MMH may be used.
- the exhaust tube 61 is provided which is connected to an exhaust apparatus 62 including a vacuum pump. By operating the exhaust apparatus 62 it is possible to reduce pressure in the chamber 11 to a predetermined vacuum level.
- a gate valve 63 is provided at the sidewall of the lower chamber 11 a and, in its open state, allows the wafer W to be passed into and out of an outside, for example, an adjacent load lock chamber, not shown.
- a coil 65 as an antenna member is wound around the upper chamber 11 b and a high frequency power source 66 is connected to the coil 65 .
- the high frequency power source 66 has a frequency of, for example, 13.65 MHz.
- a cooling mechanism 67 using a cooling medium such as a coolant and a cooling source 68 for driving this are provided.
- the gate valve 63 is opened and, in its open state, a wafer W is loaded into the chamber 11 and placed onto the electrostatic chuck 24 .
- the wafer W is attracted to the electrostatic chuck 24 by applying a voltage to the electrode 26 .
- the gate valve 63 is closed, and the interior of the chamber 11 is evacuated by the exhaust system 62 to a predetermined vacuum level.
- a high frequency power is supplied from the high frequency power source 66 to the coil 65 to create an inductive electromagnetic field within the upper chamber 11 b . Plasma is generated under this high frequency electric field.
- a predetermined amount of NH 2 gas and TiCl 4 gas are introduced into the upper chamber 11 b from the NH 3 supply source 45 and TiCl 4 supply source 44 to generate plasma and are brought to the lower chamber 11 a side.
- a TiN thin film is formed onto the wafer W.
- the formation of the TiN thin film is effected at a temperature of about 300 to 450° C. by controlling an output to the heating element 21 and an amount of flow of a coolant.
- the wafer W is unloaded out of the chamber 11 and the ClF 3 gas serving as a cleaning gas is introduced into the chamber 11 to clean the interior of the chamber.
- the inner wall of the upper chamber 11 b is attacked by the plasma generated in the upper chamber 11 b and exposed to the ClF 3 gas (etching gas) at a cleaning time.
- ClF 3 gas etching gas
- no adequate corrosion resistance was not obtained in a conventional chamber made of quartz and Al 2 O 3 with the resultant disadvantage of a short life.
- the sprayed film 14 has insulating property because it contains 6 a III-a group element of the periodic table. Use can be made of, as the basic material, various kinds of materials such as ceramic herein used, aluminum, stainless steel, rigid plastic (engineering plastic) etc. Further, the sprayed film 14 is lower in cost than a sintered product and has a greater merit of forming a film for a short period of time. It is to be noted that such sprayed film may be formed on the inner wall of the lower chamber 11 a and can enhance a corrosion resistance of the lower chamber 11 a.
- Eight types of samples were used, each comprised a 20 ⁇ 20 ⁇ 2 mm aluminum base, a 200 ⁇ m-thick first sprayed film made of Al 2 O 3 and Y 2 O 3 and formed on the aluminum base, and a 200 ⁇ m-thick second sprayed film formed on the first sprayed film.
- the first sprayed film is made of Y 2 O 3 in the first type sample, Sc 2 O 3 in the second type sample, Sc 2 F 3 in the third type sample, YF 3 in the fourth type sample, La 2 O 3 in the fifth fifty type sample, CeO 2 in the sixth type sample, Eu 2 O 3 in the seventh type sample, and DyO 3 in the eighth type sample.
- the sample was, while leaving a central area of 10 mm square, masked at its outer peripheral area with a polyimide film and irradiated with plasma.
- a plasma-resistant property was evaluated with an etched amount.
- the etched amount was evaluated with its depth, as shown in FIG. 2B, with the use of a surface roughness meter.
- samples of other materials were also evaluated in terms of the corrosion-resistant property.
- the result of evaluation is as shown in FIG. 3.
- the etched amount is shown with the etched amount of alumina standardized as “1”.
- the films containing a III-a element of the periodic table had higher corrosion resistance to plasma than the other materials.
- the sprayed film made of Al 2 O 3 and Y 2 O 3 exhibited a particularly high corrosion resistance since it was of YAG composition.
- FIGS. 4, 5 and 6 show and X-ray diffraction pattern each. As shown in these figures, for any of the sprayed films, diffraction peaks corresponding to the Al 2 O 3 and Y 2 O 3 crystals are dominant but the diffraction peaks of composite oxides, such as YAlO 3 and Y 4 Al 2 O 9 were also confirmed. It is found that the producing rate of these composite oxides is increased with an increase in the weight ratio of Al 2 O 3 /Y 2 O 3 as shown in FIG. 7.
- FIG. 10 is a cross-sectional view showing a CVD apparatus according to the second embodiment.
- a chamber, shower head and gas supply system are different in structure from those of the first embodiment.
- the same reference numerals are employed to designate parts or elements corresponding in structure to those shown in FIG. 1 and any further explanation is, therefore, omitted.
- the pipes of the gas supply system 40 are connected to the shower head member 70 .
- a pipe 81 for supplying an Ar gas and ClF 2 gas is connected to the gas discharge holes 70 a
- a pipe 82 for supplying a TiCl 4 gas and Ar gas is connected to the gas discharge holes 70 b
- a pipe 83 for supplying an NH 3 gas is connected to the gas discharge holes 70 c .
- Pipe-like gas discharge members 71 and 72 extending from the upper chamber 11 c toward the upper zone of the lower chamber 11 a are connected to the gas discharge holes 70 b and 70 c .
- a gas discharge hole 71 a is formed in the gas discharge member 71 and a gas discharge hole 72 a is formed in the gas discharge member 72 .
- a gas line 47 extending from an Ar supply source 42 and gas line 46 extending from a ClF 3 supply source 41 are connected to the pipe 81 .
- the Ar gas and ClF 3 gas are introduced from the pipe 81 into the upper chamber 11 c via the gas discharge hole 70 a , noting that the Ar gas alone is sometimes supplied there.
- a gas line 49 extending from a TiCl 4 supply source 44 and gas line 48 extending from an Ar supply source 43 are connected to the pipe 82 .
- the TiCl 4 gas using an Ar gas as a carrier gas is introduced from the pipe 82 through the gas discharge hole 70 b and gas discharge hole 71 a in the gas discharge member 71 into the upper zone of the lower chamber 11 a .
- a gas line 50 extending from an NH 3 supply source 43 is connected to the pipe 83 and the NH 3 gas is introduced from the pipe 83 through a gas discharge hole 70 c and gas discharge hole 72 a in the gas discharge member 72 into the upper zone of the lower chamber 11 a.
- the TiCl 4 gas and NH 3 gas are supplied directly into the upper zone of the lower chamber 11 a without passing through the upper chamber 11 c . After so discharged, these gases are mixed within the lower chamber 11 a .
- the gas line 46 extending from the ClF 3 supply source 41 is joined into the gas line 81 and, by opening a valve 51 on the gas line 46 , the ClF 3 as a cleaning gas is supplied past the gas line 46 and then the pipe 81 to the shower head 70 to allow the ClF 3 gas to be introduced via the discharge hole 70 a into the upper chamber 11 c.
- a wafer W is loaded into the chamber 11 and the Ar gas as a plasma generation gas is introduced via the gas discharge holes 70 a in the shower head into the upper chamber 11 c .
- the Ar gas as a plasma generation gas is introduced via the gas discharge holes 70 a in the shower head into the upper chamber 11 c .
- the film-formed semiconductor wafer is externally unloaded out of the chamber 11 and a ClF 3 gas serving as a cleaning gas is introduced into the chamber 11 to clean the inner wall of the chamber.
- the Ar gas alone for plasma generation is supplied into the upper chamber 11 c and the TiCl 4 gas and NH 3 gas, serving as a process gas, are supplied directly into the lower chamber 11 a via the gas discharge members 71 and 72 , so that the process gas almost never reaches the inner wall of the upper chamber 11 c . As a result, almost no deposit resulting from the process gas is formed on the inner wall of the upper chamber 11 c.
- FIG. 11 is a cross-sectional view showing a CVD apparatus according to a third embodiment of the present invention.
- This embodiment constitutes a combined structure of a lower chamber 11 a similar to that in the first embodiment shown in FIG. 1 and an upper chamber 11 c similar to that of the second embodiment shown in FIG. 10.
- a sprayed film 14 of mainly Al 2 O 3 and Y 2 O 3 having an insulating property and high corrosion resistance as set out above is formed on the inner wall of the upper chamber 11 b .
- the same reference numerals are employed to designate parts or elements corresponding in structure to those shown in FIGS. 1 and 10 and any further explanation is, therefore, omitted.
- a high-corrosion-resistant sprayed film 14 is formed on the inner wall of the upper chamber 11 c and, even if plasma and cleaning gas are contacted with the inner wall, is hard to be etched to provide a longer service life to the chamber. In addition, almost no deposit resulting from the process gas is formed on the upper chamber 11 b . As a result, unlike the prior art technique, there is no inconvenience of the plasma being attenuated by a conductive film deposited on the inner wall of the chamber and hence no difficulty is encountered in the formation of a film.
- a sprayed film may be formed on the inner wall of the lower chamber 11 a and, by forming such a sprayed film, it is possible to improve a high corrosion resistance to the lower chamber 11 a.
- a gas supplied from the gas supply system 40 is discharged and directed toward a central area at the upper zone of the lower chamber 11 a and diffused onto a wafer W.
- a deposit resulting from a process gas is almost hardly formed on the inner wall of the upper chamber 11 d .
- a sprayed film 14 is formed on the inner wall of the upper chamber and, even if plasma and cleaning gas are contacted with the inner wall, etching is less liable to occur and it is possible to extend the service life of the chamber.
- FIGS. 13A and 13B each shows a practical structure of a shower head 81 in this embodiment.
- the shower head 81 is comprised of a ring-type three-layered structure and so designed as to collect gases in the respective outer head sections into a middle-layer head section. That is, ring-like diffusion channels 84 a , 85 a and 86 a are provided in the head sections 84 , 85 and 86 to allow the process gas to be introduced into the chamber.
- a plurality of discharge holes 84 b (NH 3 gas), discharge holes 85 b (Ar gas) and discharge holes 86 b (TiCl 4 gas or ClF 3 gas) leading to the diffusion channels 84 a , 85 a and 86 a are provided in a middle layer of the head section 85 in one array to allow a corresponding gas to be discharged in a horizontal direction.
- these discharge holes are so arranged as to allow different kinds of process gases to be sequentially discharged with an argon gas in between.
- the discharge holes 85 b , 86 b , 85 b , 84 b , 85 b , 86 b , . . . that is, an Ar gas, TiCl 4 gas or ClF 3 gas, Ar gas, NH 3 gas, Ar gas, TiCl 4 gas or ClF 3 gas, . . . are used.
- FIG. 15 Various practical structures as shown in FIG. 15 are realized depending upon the order in which these head sections are stacked. In these structures, six cases are shown in FIG. 15. It is to be noted that the TiCl 4 gas and ClF 3 gas are switchingly used at a film forming time and cleaning time but that independent corresponding discharge holes may be provided for these gases.
- the shower heads for introducing the gases into the chamber can be variously changed or modified in the embodiment of the present invention.
- a shower head is so configured as to have one gas introducing member 95 for allowing a process gas to be supplied from the top side of an upper bell jar onto a wafer W within a lower chamber and a gas discharge section 96 connected to the lower end of the gas introducing member 95 and having a plurality of discharge holes to allow a gas to be spirally supplied down toward the wafer W.
- a shower head comprises one gas introducing member 97 similar to the gas introducing member 95 and a plurality of gas discharge sections 98 connected to the lower end of the gas introducing member 97 , provided in an outwardly branched fashion and having a plurality of discharge holes so provided as to allow a gas to be discharged down onto a wafer W.
- two kinds of process gases are separately individually introduced into the chamber, these gases may be introduced together.
- the present invention is not restricted thereto and other films may be formed.
- a Cl-containing gas is used as a feed gas and the present invention is effective to the formation of a film using these materials.
- TiN, Ti, TiSiN, SiN, Ta, TaN, Ta 2 O 5 , PZT, BST, RuO and ZrO As such materials, use is made of, for example, TiN, Ti, TiSiN, SiN, Ta, TaN, Ta 2 O 5 , PZT, BST, RuO and ZrO; a LOWK material, such as SiOF recently used as an insulating interlayer of a low dielectric constant; and Ta, TaN used as a barrier of Cu and SiN used as a etching stop.
- FIGS. 18, 19 and 20 Those applied forms of chambers provided in the processing apparatus according to the above-mentioned embodiments will be explained below with reference to FIGS. 18, 19 and 20 .
- the lower chamber 11 a shown in FIG. 1 is taken as an example and, as a gas supply system, a gas supply system for supplying a gas from the sidewall of the chamber shown in FIG. 12 is taken as an example.
- a gas supply system for supplying a gas from the sidewall of the chamber shown in FIG. 12 is taken as an example.
- FIG. 18 is one example of a lower-height thin type chamber.
- This thin type chamber 11 e is thin and has a height (depth) H of, for example, about 0.65 to 10 cm and, preferably, 0.65 to 5 cm.
- the distance from the inner top surface of the chamber to a wafer W is about 3.8 to 30 cm and, preferably, 3.8 to 20 cm. Since, in this way, the chamber has a lower-volume shape, an exposed area within the chamber is smaller and hence the apparatus is smaller and ensures an easier maintenance. It is, therefore, possible to alleviate an evacuation load on the system 62 .
- An upper chamber 11 f shown in FIG. 19 is of a semi-spherical type, that is, a bell jar type and an upper chamber 11 g shown in FIG. 20 is of a dome-shaped type. According to these upper chambers, the distribution of an electric field by an antenna relative to the wafer W is made uniform compared with that of a box-type chamber and hence the thickness profile of a formed film, etching, etc., are made uniform.
- FIG. 21 is a view showing a practical structure applied to a heat processing apparatus as a fifth embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
- the heat processing apparatus 101 can perform an anneal process for promoting recrystallization of a formed film and a thermal oxidation process.
- This heat processing apparatus 101 has a susceptor 103 located within a chamber 102 to support a wafer W, a wafer lifting mechanism 105 provided below the susceptor 103 to allow the wafer W to be lifted up by a plurality of lift pins 104 at a transfer of the wafer W, a heater 106 provided in the susceptor 103 and a gas flow chamber 107 for hermetically supplying a gas such as an Ar gas and oxygen gas onto the wafer W.
- a gas flow chamber 107 for hermetically supplying a gas such as an Ar gas and oxygen gas onto the wafer W.
- a sprayed film 14 of Al 2 O 3 /Y 2 O 3 is formed on the inner surface of the gas flow chamber 107 and on the surface of a guide section 108 provided on the susceptor 103 to guide a wafer mounting position and, by doing so, it is possible to obtain the same effect as in the above-mentioned respective embodiments.
- FIG. 22 is a view showing a practical structure applied to an ashing apparatus as a sixth embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
- the ashing apparatus comprises a hermetically sealable chamber 111 having a lower chamber 111 a and upper chamber 111 b , a susceptor 112 on which a wafer W is placed, a heater 113 provided in the susceptor 112 to heat the wafer W, a gas supply system, not shown, for supplying a process gas such as oxygen, and an evacuation apparatus for evacuating the interior of the chamber 111 .
- a high-corrosion-resistant sprayed film is formed on the whole inner surface of the upper chamber 111 b and on the sidewall of the lower chamber 111 a except the inner bottom surface and, by doing so, it is possible to obtain the same effect as in the above-mentioned respective embodiment.
- FIG. 23 is a view showing a practical structure applied to an etching apparatus as a seventh embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
- a sprayed film 14 is formed, as the above-mentioned case, on exposed surfaces of the susceptor 123 , focusing ring 130 , shower head 122 and shield ring 128 within the chamber and further on the inner upper surface and inner bottom surface of the chamber 121 .
- a sprayed film of substantially Al 2 O 3 /Y 2 O 3 whose weight ratio is above 0.5 is formed on the inner wall of the chamber and, by doing so, the chamber is less liable to be etched under a plasma and cleaning gas due to the presence of the high-corrosion resistant sprayed film.
- the present invention can be preferably applied to the film formation, etching, ashing and heat treatment on a less-etching thermal sprayed film of the chamber.
- the gas supply system supplies a process gas near the upper zone of a wafer within the chamber, the gas hardly reaches the inner wall of the chamber and almost no product is deposited on the wall.
- a material for the chamber use can be made of a ceramic (Al 2 O 3 , SiO 2 , AlN, etc.), aluminum, stainless steel, metal or alloy.
Abstract
A processing apparatus of the present invention has a mounted chamber holding a semiconductor wafer and having members for work-processing the substrate under any of heating, plasma and process gas or a combination of them, in which a film of Al2O3 and Y2O3 is formed on an inner wall surface of the chamber and on those exposed surface of the members within the chamber and has a high-corrosion resistance and insulating property and, when the process gas is introduced onto a processing surface of a semiconductor wafer and diffused into it, any product is less liable to be deposited on a plasma generation area and on those members held within the chamber.
Description
- This application is based upon and claims the benefit of priority from the prior Japanese Patent Application No. 11-352018, filed Dec. 10, 1999, the entire contents of which are incorporated herein by reference.
- A present invention relates to a processing chamber having a mounted chamber having a high-corrosion-resistant film and applied to a film forming apparatus, heat processing apparatus and etching apparatus as used in a CVD (Chemical Vapor Deposition), etc.
- In response to a recent demand for a high density and high integration unit, a semiconductor device is progressed from a two-dimensional connection structure toward a three-dimensional multi-connection structure. For this reason, the burying technique for electrical interlayer connection using a contact hole for connection between an underlying circuit element and an overlying connection layer and a via hole for connection between an underlying connection layer and an overlying connection layer, and so on, is becoming important. For the burying of the contact hole and via hole, use is made of Al (aluminum), W (tungsten) or an alloy including these as a main component.
- At the burying step using aluminum or aluminum alloy, a heating step and so on are involved during a manufacture. If the aluminum connection line and underlying silicon (Si) substrate are directly contacted with each other, there is a risk that there will occur a “Si-sucking-up” effect of aluminum, etc., at its boundary area and an alloy will be newly formed there. The alloy thus formed is greater in the value of a resistance and is not desirable from the standpoint of a power saving and high-speed operation demanded of a resultant device. Further, when tungsten or tungsten alloy is used as a burying layer in the contact hole, WF6 gas intrudes into the silicon substrate, thus offering a possibility of deteriorating the electrical characteristic, etc., of the device. This is, therefore, not preferable.
- In order to prevent the occurrence of such a problem, a barrier layer is formed on the bottom and inner wall of the hole before forming a buried layer in the contact hole or via hole and then such a buried layer is formed. Generally, a TiN film is known as a barrier layer.
- With a trend toward the high-density integration, on the other hand, a high dielectric constant material such as Ta2O5 is used as a capacitor gate material to obtain a higher capacitance without changing its scale. However, such a higher dielectric constant material is not stabler in characteristic than SiO2 conventionally used as the capacitor gate material. If a poly-Si is used on the overlying electrode, it is oxidized due to the chemical reaction after the formation of the capacitance, thus failing to manufacture a device element of stable characteristics. It is, therefore, necessary that a less-oxidized TiN film be used as an overlying electrode.
- The TiN film has been formed by using a physical vapor deposition (PVD) technique and a demand has been made for a finer and higher integration device in particular. In addition, the design rules are particularly stringent. Hence, in PVD that can hardly achieve high coverage. Therefore, a chemical vapor deposition (CVD) technique is used by which it is possible to form a TiN film of a better quality. Stated in more detail, a thermal CVD is used, in which TiCl4 and NH3 (ammonia) or MMH (monomethylhydrazine) is applied, as a reaction gas, to a heated substrate. In the case where the TiN film is formed by such a thermal CVD, chlorine is liable to be retained in a formed film, thus presenting a problem. The retaining of such chlorine results in a higher specific resistance and it is not possible to obtain a proper characteristic if the film is applied to an electrode overlying a capacitor.
- Further, the TiN film, being a columnar crystal, is liable to be boundary-diffused and involves a lower barrier characteristic. The lower barrier characteristic presents a problem in the case where the TiN film is used as a barrier layer for a Cu connection line or an oxygen diffusion barrier for Ta2O5 connection line of an electrode overlying the capacitor. That is, a problem occurs due to the corrosion of the Cu connection line by the residual chlorine or a lowering of a capacitance of Ta2O5 by the diffusion of oxygen.
- An amount of Cl in the formed film can be indeed reduced by making a film formation temperature higher. However, a high temperature process is not preferable due to a problem, such as thermal resistance and the corrosion, of a connection line material such as Cu and Al.
- As one technique of plasma CVD, there is an ICP (Inductively Coupled Plasma)—CVD according to which an antenna member such as a coil is provided around a bell jar (chamber). By applying a high frequency power to it, an inductive electromagnetic field is created to provide plasma. In the case where the TiN film is formed using this technique, the formed TiN film becomes low-resistance and low in chlorine, and even a film formed at a relatively low temperature is made low in an amount of residual chlorine.
- Although a chamber made of quartz or alumina is used in the formation of the TiN film by the ICP-CVD, it is not good in a plasma-resistant characteristic and a corrosion resistance to an etching gas such as ClF3 used for cleaning the interior of the apparatus after the formation of the TiN film is not better, thus presenting a problem.
- Further, in this type of CVD film formation apparatus, a deposit is formed on the inner wall of the chamber due to the introduction of a process gas from above the chamber and a foreign deposit is liable to be formed. In the case of forming the TiN film, the plasma created is attenuated due to the deposit of a conductive film on the inner wall of the upper chamber, thus making it difficult to form a film.
- An object of the present invention is to provide a processing apparatus having a chamber applied to a film forming apparatus, heat processing apparatus and etching apparatus and having a high-corrosion-resistant property and less liable to deposit a product by a process gas or a product, such as an etching product, on its inner wall thereof.
- The thus constructed processing apparatus has a mounted chamber holding a to-be-processed substrate and having members for work-processing the substrate by any of heating, plasma, process gas or a combination thereof, in which a film of Al2O3 and Y2O3 is formed on the inner wall surface of the chamber and on the exposed surfaces of the members within the chamber, the Al2O3/Y2O3 weight ratio being above 0.5. The Al2O3/Y2O3 weight ratio is in a range above 0.5 but below 4. The thickness of the formed film is above 50 μm.
- Additional objects and advantages of the invention will be set forth in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention. The objects and advantages of the invention may be realized and obtained by means of the instrumentalities and combinations particularly pointed out hereinafter.
- The accompanying drawings, which are incorporated in and constitute a part of the specification, illustrate presently preferred embodiments of the invention, and together with the general description given above and the detailed description of the preferred embodiments given below, serve to explain the principles of the invention.
- FIG. 1 is a view showing a practical structure of a plasma CVD apparatus according to a first embodiment of the present invention;
- FIGS. 2A and 2B are views showing a sample of a test by etching and evaluation standard;
- FIG. 3 is a view showing a relation of members in an etching time to an etched amount;
- FIG. 4 is a view showing an X-ray diffraction pattern of a sprayed film when an Al2O3/Y2O3 weight ratio=0.43;
- FIG. 5 is a view showing an X-ray diffraction pattern of a sprayed film when an Al2O3/Y2O3 weight ratio=0.66;
- FIG. 6 is a view showing an X-ray diffraction pattern of a sprayed film when an Al2O3/Y2O3 weight ratio=1.50;
- FIG. 7 is a view showing a rate of a composite oxide when the Al2O3/Y2O3 weight ratio of a sprayed film varies;
- FIG. 8 is a view showing a relation of an Al2O3/Y2O3 weight ratio of a sprayed film to an etched amount;
- FIG. 9 is a view showing an X-ray diffraction pattern of a sprayed film when sprayed is made using a YAG;
- FIG. 10 is a view showing a practical form of a plasma CVD apparatus according to a second embodiment;
- FIG. 11 is a view showing a practical form of a plasma CVD apparatus according to a third embodiment;
- FIG. 12 is a view showing a practical structure of a plasma CVD apparatus according to a fourth embodiment;
- FIGS. 13A and 13B show a practical structure of a shower head in the fourth embodiment;
- FIGS. 14A and 14B are a view showing a modified structure of the shower head in the fourth embodiment;
- FIG. 15 is a view showing practical structures of head section;
- FIG. 16 is a perspective view showing a first modified structure of a gas discharge member;
- FIG. 17 is a perspective view showing a second modified structure of a gas discharge member;
- FIG. 18 is a view showing one form of a lower-height thin type chamber;
- FIG. 19 is a view showing one form of a semi-spherical type chamber;
- FIG. 20 is a view showing one form of a dome-type chamber;
- FIG. 21 is a view showing a practical structure of a heat processing apparatus;
- FIG. 22 is a view showing a practical structure of an ashing apparatus;
- FIG. 23 is a view showing a practical structure of an etching apparatus; and
- FIG. 24 is a view showing a relation of a breakdown voltage to the thickness of the sprayed film in the respective embodiment of the present invention.
- The embodiments of the present invention will be described below with reference to the accompanying drawings.
- FIG. 1 is a cross-sectional view showing a practical example applied to a CVD film forming apparatus as a first embodiment of the present invention in a processing apparatus having a mounted chamber having a high corrosion-resistant thermal sprayed film.
- The film forming apparatus of the present invention is directed to forming, for example, a TiN thin film. The
film forming apparatus 10 includes achamber 11 having alower chamber 11 a andupper chamber 11 formed as an integral unit in a hermetically sealable way. Theupper chamber 11 b is made smaller in diameter than thelower chamber 11 a. Thelower chamber 11 a is comprised of anelectric conductor 12, such as aluminum, whose surface is anadigation processed for example. Theupper chamber 11 b comprises abase material 13 of, for example, a ceramic material and a sprayedfilm 14. Thefilm 14 may contain oxide of Y, Sc, La, Ce, Eu, Dy or the like, or fluoride of one of these metals. Thefilm 14 may be made of a compound of a III-a element of the periodic table, such as Y2O3. Needless to say, thefilm 14 may be made of such a compound and any other material. In the present invention, thefilm 14 containing a compound of a III-a element is a sprayed film that substantially comprises Al2O3 and Y2O3. As the material of the chamber use can be made of ceramic (Al2O3, SiO2, AlN etc.,), aluminum or stainless steel, metal or metal alloy. - A weight ratio of Al2O3/Y2O3 of the sprayed
film 14 is preferably 0.5 to 4. It is to be noted that FIG. 8 simply shows data of the weight ratio of up to 1.5. In the formation of the sprayedfilm 14 it may be possible to spray an Al2O3 and Y2O3 compound or to spray, for example, yttrium-aluminum-garnet (YAG) in a composite oxide state of the above-mentioned composition range. The thickness of the sprayed film is based on the insulation withstand characteristic for plasma generation and, from the standpoint of the breakdown voltage characteristic shown in, for example, FIG. 2, may be of the order of at least 50 μm and preferably of the order of 50 μm but not above 300 μm from the standpoint of a manufacturing process and cost. - The ceramics of the
base material 13 may be Al2O3, SiO2, such as silica glass and quartz, AlN, alternatively, rigid plastic may be used, and, here, the sprayed film as set out above is not formed on the inner wall of theupper chamber 11 b but it may be formed there. - On the inner bottom of the
lower chamber 11 a an insulatingplate 15 of ceramic, etc., andsupport base 16 are provided and a substantiallycylindrical susceptor 17 is provided on thesupport base 16 to place a semiconductor wafer (hereinafter referred to as a wafer) as a to-be-processed object on it. - A
coolant chamber 18 is provided in the interior of thesupport base 16 to receive the coolant via acoolant introducing tube 19. The coolant is discharged out of adischarge tube 20. Through such a circulation, a cold is conducted through thesusceptor 17 to the wafer W.A heating element 21 is buried in thesusceptor 17 to heat the wafer W to a predetermined temperature by supplying power from apower source 22. To thepower source 22, acontroller 23 is connected. And the temperature of the wafer W is controlled by a cold of the coolant and heat of the heating element. - At the
susceptor 17, anelectrostatic chuck 24 is provided which is substantially the same in configuration as the wafer W. Theelectrostatic chuck 24 is so formed as to have anelectrode 26 buried in an insulatingmaterial 25. The wafer W is electrostatically attracted by a Coulomb force, etc., generated by applying a DC voltage from aDC power source 27 to theelectrode 26. At the outer peripheral portion of an upper surface of theelectrostatic chuck 24 an area for achieving the uniformity of a film formation, for example, a focusingring 28 is provided to surround the wafer W. The above-mentioned sprayedfilm 14 is formed on those exposed surfaces of thesupport base 16,susceptor 17,electrostatic chuck 24 and focusingring 28 within the chamber. - A
shower head member 30 is provided above thechamber 11 b. In theshower head member 30, many gas discharge holes 30 a (Ar, ClF3), 30 b (Ar, TiCl4) and 30 c (NH3) are alternately formed to discharge gases in a down direction within the chamber. The pipes of agas supply system 40 are connected to theshower head member 30. That is, as will be set out below, apipe 55 for supplying a gas (Ar, ClF3) is connected to the gas discharge holes 30 a, apipe 56 for supplying a gas (Ar, TiCl4) is connected to the gas discharge holes 30 b and a pipe 57 for supplying a gas (NH3) is connected to the gas discharge holes 30 c. By doing so, the respective gases are introduced through theshower head member 30 into theupper chamber 11 b. - The
shower head member 30 is comprised of, for example, a three-layers-stacked structure of three gas dispersion plate and has discharge plate having the gas discharge holes. The respective gas discharge plate has a groove and holes for allowing one kind of gas to be dispersed evenness to a whole gas discharge surface area in the head. In particular, the discharge holes of the gas dispersion plate are so formed as not be overlapped with the discharge holes of the other gas dispersion plate. Though being not illustrated in the Figure, the gas discharge holes are arranged in a matrix array upon viewing the gas discharge hole surface side from below. And a post-mixing system is adopted according to which TiCl4 gas and NH3 gas are discharged from the alternately formed different discharge holes and these gases are mixed as a process gas after being discharged. - The
gas supply system 40 has a ClF3 supply source 41 for supplying ClF3 as a cleaning gas,Ar supply sources gas line 46 is connected to the ClF3 supply source 41,gas lines Ar supply sources gas line 49 is connected to the TiCl4 supply source 44 and agas line 50 is connected to the NH3 supply source 45. A valve 51 (51 a, 51 b) andmass flow controller 52 are provided at these gas lines. - Into the
gas line 47 extending from theAr supply source 42, thegas line 46 extending from the ClF3 supply source 41 is joined and thegas line 46 extending form the ClF3 supply source 41 is joined. Thegas line 46 extending form the ClF3 supply source 41 is joined into agas line 53. By opening thevalve 51 provided on thegas line 46, ClF3 serving as a cleaning gas is passed through thegas line 46 andpipe 53 and reaches theshower head 30 to allow it to be introduced via the gas discharge holes 30 a into theupper chamber 11 b. Needless to say, there is the case where Ar alone is supplied from theAr supply source 42. - Into the
gas line 48 extending from theAr supply source 43, thegas line 49 extending from the TiCl4 supply source 44 is joined. TiCl4 gas passed through thegas line 49 andpipe 54 is carried by the argon gas and reaches theshower head 30. The TiCl4 gas is introduced from the gas discharge holes 30 b into thechamber 11. - Further, the NH3 gas is supplied from the NH3 supply source 45 past the
gas line 50 andpipe 55 to theshower head 30 and introduced from the gas discharge holes 30 c into theupper chamber 11 b. It is to be noted that, in place of NH3, monomethylhydrazine (MMH) may be used. - At the bottom wall of the
lower chamber 11 a theexhaust tube 61 is provided which is connected to anexhaust apparatus 62 including a vacuum pump. By operating theexhaust apparatus 62 it is possible to reduce pressure in thechamber 11 to a predetermined vacuum level. Agate valve 63 is provided at the sidewall of thelower chamber 11 a and, in its open state, allows the wafer W to be passed into and out of an outside, for example, an adjacent load lock chamber, not shown. - A
coil 65 as an antenna member is wound around theupper chamber 11 b and a highfrequency power source 66 is connected to thecoil 65. The highfrequency power source 66 has a frequency of, for example, 13.65 MHz. By supplying a high frequency power from the highfrequency power source 66 to thecoil 65 an inductive electromagnetic field is created within theupper chamber 11 b. Further, acooling mechanism 67 using a cooling medium such as a coolant and acooling source 68 for driving this are provided. - With this apparatus, the
gate valve 63 is opened and, in its open state, a wafer W is loaded into thechamber 11 and placed onto theelectrostatic chuck 24. The wafer W is attracted to theelectrostatic chuck 24 by applying a voltage to theelectrode 26. Thereafter, thegate valve 63 is closed, and the interior of thechamber 11 is evacuated by theexhaust system 62 to a predetermined vacuum level. Then, while introducing an Ar gas from theAr supply source 42 into thechamber 11, a high frequency power is supplied from the highfrequency power source 66 to thecoil 65 to create an inductive electromagnetic field within theupper chamber 11 b. Plasma is generated under this high frequency electric field. - Then, a predetermined amount of NH2 gas and TiCl4 gas are introduced into the
upper chamber 11 b from the NH3 supply source 45 and TiCl4 supply source 44 to generate plasma and are brought to thelower chamber 11 a side. By this plasma, a TiN thin film is formed onto the wafer W. At this time, the formation of the TiN thin film is effected at a temperature of about 300 to 450° C. by controlling an output to theheating element 21 and an amount of flow of a coolant. After the film formation, the wafer W is unloaded out of thechamber 11 and the ClF3 gas serving as a cleaning gas is introduced into thechamber 11 to clean the interior of the chamber. - In the above-mentioned processing, the inner wall of the
upper chamber 11 b is attacked by the plasma generated in theupper chamber 11 b and exposed to the ClF3 gas (etching gas) at a cleaning time. Under such an environment, no adequate corrosion resistance was not obtained in a conventional chamber made of quartz and Al2O3 with the resultant disadvantage of a short life. According to the present invention, however, use is made mainly of Al2O3 and Y2O3 and a high-corrosion-resistant sprayedfilm 14 having Al2O3/Y2O3 weight ratio of above 0.5 is formed on the inner wall of theupper chamber 11 b. Hence, even if being contacted with plasma and cleaning gas, the inner wall of the chamber is less likely to be etched and ensures a longer service life. - The sprayed
film 14 has insulating property because it contains 6 a III-a group element of the periodic table. Use can be made of, as the basic material, various kinds of materials such as ceramic herein used, aluminum, stainless steel, rigid plastic (engineering plastic) etc. Further, the sprayedfilm 14 is lower in cost than a sintered product and has a greater merit of forming a film for a short period of time. It is to be noted that such sprayed film may be formed on the inner wall of thelower chamber 11 a and can enhance a corrosion resistance of thelower chamber 11 a. - An explanation will be made below about the results of experiments by which the corrosion resistance of the sprayed film is confirmed. Here, a parallel flat type plasma etching apparatus was used by way of example. A strayed film was irradiated, with plasma, at an intra-chamber pressure of 133.3 Pa (1000m Torrs) and a gas flow rate of CF4: Ar:O2=95: 950:10 (a total flow rate of 0.0633 m3/sec (1055 sccm)) for 20 hours through the application of a high frequency power of 13.56 MHz at 1300 W.
- Eight types of samples were used, each comprised a 20×20×2 mm aluminum base, a 200 μm-thick first sprayed film made of Al2O3 and Y2O3 and formed on the aluminum base, and a 200 μm-thick second sprayed film formed on the first sprayed film. The first sprayed film is made of Y2O3 in the first type sample, Sc2O3 in the second type sample, Sc2F3 in the third type sample, YF3 in the fourth type sample, La2O3 in the fifth fifty type sample, CeO2 in the sixth type sample, Eu2O3 in the seventh type sample, and DyO3 in the eighth type sample. Stated in more detail, use was made of a sprayed film having a weight ratio of Al2O3/Y2O3=0.5 and a film sprayed with a 99.9%-purity YAG (Y3Al5O12 a weight ratio of Al2O3/Y2O3=0.75). As shown in FIG. 2A, the sample was, while leaving a central area of 10 mm square, masked at its outer peripheral area with a polyimide film and irradiated with plasma. And a plasma-resistant property was evaluated with an etched amount. The etched amount was evaluated with its depth, as shown in FIG. 2B, with the use of a surface roughness meter. For comparison, samples of other materials were also evaluated in terms of the corrosion-resistant property. The result of evaluation is as shown in FIG. 3. Here, the etched amount is shown with the etched amount of alumina standardized as “1”.
- It was confirmed that, as shown in FIG. 3, the films containing a III-a element of the periodic table had higher corrosion resistance to plasma than the other materials. Of these films, the sprayed film made of Al2O3 and Y2O3 exhibited a particularly high corrosion resistance since it was of YAG composition.
- Then, with an Al2O3/Y2O3 weight ratio set to 0.43, 0.66, and 1.5, these mixed powders were sprayed onto an aluminum basic material to form a sprayed film. FIGS. 4, 5 and 6 show and X-ray diffraction pattern each. As shown in these figures, for any of the sprayed films, diffraction peaks corresponding to the Al2O3 and Y2O3 crystals are dominant but the diffraction peaks of composite oxides, such as YAlO3 and Y4Al2O9 were also confirmed. It is found that the producing rate of these composite oxides is increased with an increase in the weight ratio of Al2O3/Y2O3 as shown in FIG. 7.
- In the same way as set out above, these samples were tested for corrosion resistance to plasma. The evaluation of the etched amount was made by measuring its depth at a central portion of the above-mentioned 10 mm square portion except the edge portion. The result is as shown in FIG. 8. From this Figure it is found that, with an Al2O3/Y2O3 weight ratio of above 0.5, the corrosion resistance is better. Since, as set out above, with an increase in the weight ratio of Al2O3/Y2O3, the production rate of the composite oxide is increased, there is a possibility that the composite oxide contributes to the corrosion resistance.
- On the other hand, the YAG sprayed film evaluated for the corrosion resistance at the first test was substantially amorphous as shown in FIG. 9.
- From this it may be considered that the corrosion resistance is improved by making the sprayed film amorphous.
- A second embodiment of the present invention will be explained below.
- FIG. 10 is a cross-sectional view showing a CVD apparatus according to the second embodiment. In this embodiment, a chamber, shower head and gas supply system are different in structure from those of the first embodiment. In this Figure, the same reference numerals are employed to designate parts or elements corresponding in structure to those shown in FIG. 1 and any further explanation is, therefore, omitted.
- In this apparatus, an
upper chamber 11 c is provided above alower chamber 11 a and it is made of a ceramic material, such as Al2O3, SiO2 and AlN. At ashower head member 70 of pipe type provided at the top of theupper chamber 11 c, gas discharge holes 70 a, 70 b and 70 c are alternately formed to discharge gases toward a lower zone within the chamber. A gas supply system 40 a comprises gas supply sources andvalves 51 andmass flow controllers 52 as in the case of thegas supply system 40 as set out above. This embodiment is different from the first embodiment with respect to a pipe array from thegas supply system 40 to theshower head member 70. - That is, the pipes of the
gas supply system 40 are connected to theshower head member 70. As will be set out below, apipe 81 for supplying an Ar gas and ClF2 gas is connected to the gas discharge holes 70 a, apipe 82 for supplying a TiCl4 gas and Ar gas is connected to the gas discharge holes 70 b, and a pipe 83 for supplying an NH3 gas is connected to the gas discharge holes 70 c. Pipe-likegas discharge members upper chamber 11 c toward the upper zone of thelower chamber 11 a are connected to the gas discharge holes 70 b and 70 c. Agas discharge hole 71 a is formed in thegas discharge member 71 and agas discharge hole 72 a is formed in thegas discharge member 72. - A
gas line 47 extending from anAr supply source 42 andgas line 46 extending from a ClF3 supply source 41 are connected to thepipe 81. The Ar gas and ClF3 gas are introduced from thepipe 81 into theupper chamber 11 c via thegas discharge hole 70 a, noting that the Ar gas alone is sometimes supplied there. - A
gas line 49 extending from a TiCl4 supply source 44 andgas line 48 extending from anAr supply source 43 are connected to thepipe 82. The TiCl4 gas using an Ar gas as a carrier gas is introduced from thepipe 82 through the gas discharge hole 70 b andgas discharge hole 71 a in thegas discharge member 71 into the upper zone of thelower chamber 11 a. Agas line 50 extending from an NH3 supply source 43 is connected to the pipe 83 and the NH3 gas is introduced from the pipe 83 through agas discharge hole 70 c andgas discharge hole 72 a in thegas discharge member 72 into the upper zone of thelower chamber 11 a. - Thus, the TiCl4 gas and NH3 gas are supplied directly into the upper zone of the
lower chamber 11 a without passing through theupper chamber 11 c. After so discharged, these gases are mixed within thelower chamber 11 a. Thegas line 46 extending from the ClF3 supply source 41 is joined into thegas line 81 and, by opening avalve 51 on thegas line 46, the ClF3 as a cleaning gas is supplied past thegas line 46 and then thepipe 81 to theshower head 70 to allow the ClF3 gas to be introduced via thedischarge hole 70 a into theupper chamber 11 c. - In the thus structured CVD apparatus, a wafer W is loaded into the
chamber 11 and the Ar gas as a plasma generation gas is introduced via the gas discharge holes 70 a in the shower head into theupper chamber 11 c. By supplying a high frequency power from a highfrequency power source 66 to acoil 65, an inductive electromagnetic field is created within theupper chamber 11 c to generate a plasma of the Ar gas. - On the other hand, the TiCl4 gas and NH3 gas serving as a process gas are directly introduced into the upper zone of the
lower chamber 11 a via thedischarge members upper chamber 11 c into thelower chamber 11 a. By doing so, the gases generate a plasma at the upper zone of thelower chamber 11 a, so that a reaction occurs on the surface of the wafer W to form a TiN thin film on the wafer. - Even in this embodiment, the film-formed semiconductor wafer is externally unloaded out of the
chamber 11 and a ClF3 gas serving as a cleaning gas is introduced into thechamber 11 to clean the inner wall of the chamber. - In this embodiment, as set out above, the Ar gas alone for plasma generation is supplied into the
upper chamber 11 c and the TiCl4 gas and NH3 gas, serving as a process gas, are supplied directly into thelower chamber 11 a via thegas discharge members upper chamber 11 c. As a result, almost no deposit resulting from the process gas is formed on the inner wall of theupper chamber 11 c. - Thus, unlike the prior art technique, a conductive film is not deposited, by the process gas, on the inner wall of the chamber and it is never difficult to form a film under the attenuation of plasma involved.
- A third embodiment of the present invention will be described below.
- FIG. 11 is a cross-sectional view showing a CVD apparatus according to a third embodiment of the present invention.
- This embodiment constitutes a combined structure of a
lower chamber 11 a similar to that in the first embodiment shown in FIG. 1 and anupper chamber 11 c similar to that of the second embodiment shown in FIG. 10. A sprayedfilm 14 of mainly Al2O3 and Y2O3 having an insulating property and high corrosion resistance as set out above is formed on the inner wall of theupper chamber 11 b. In this embodiment, the same reference numerals are employed to designate parts or elements corresponding in structure to those shown in FIGS. 1 and 10 and any further explanation is, therefore, omitted. - In the third embodiment, a high-corrosion-resistant sprayed
film 14 is formed on the inner wall of theupper chamber 11 c and, even if plasma and cleaning gas are contacted with the inner wall, is hard to be etched to provide a longer service life to the chamber. In addition, almost no deposit resulting from the process gas is formed on theupper chamber 11 b. As a result, unlike the prior art technique, there is no inconvenience of the plasma being attenuated by a conductive film deposited on the inner wall of the chamber and hence no difficulty is encountered in the formation of a film. - It is to be noted that, even in the second and third embodiments, a sprayed film may be formed on the inner wall of the
lower chamber 11 a and, by forming such a sprayed film, it is possible to improve a high corrosion resistance to thelower chamber 11 a. - A fourth embodiment of the present invention will be explained below.
- FIG. 12 is a cross-sectional view showing a CVD apparatus according to the fourth embodiment of the present invention.
- The apparatus structure of this embodiment comprises a combination of a
lower chamber 11 a similar to that of the above-mentioned first embodiment and an upper chamber lid different in gas supply position above thelower chamber 11 a. In this embodiment, the same reference numerals are employed to designate parts or elements corresponding in structure to those shown in FIG. 1 and any further explanation is, therefore, omitted. - In this film forming apparatus, a
shower head 81 for supplying a process gas into achamber 11 is formed in an annular shape between the upper chamber 11 d and thelower chamber 11 a. A high corrosion-resistant and insulating sprayedfilm 14 is formed on the whole inner surface of the upper chamber 11 d. Agas supply system 40 is similar in structure to that of the first embodiment but a ClF3 gas serving as a cleaning gas and Ar gas can be introduced from the top side and sidewall side of the upper chamber 11 d by a switching operation of thevalves 82 and 83. - By this structure, a gas supplied from the
gas supply system 40 is discharged and directed toward a central area at the upper zone of thelower chamber 11 a and diffused onto a wafer W. In this embodiment, it is possible to obtain an effect similar to that of the above-mentioned embodiments. And a deposit resulting from a process gas is almost hardly formed on the inner wall of the upper chamber 11 d. Further, a sprayedfilm 14 is formed on the inner wall of the upper chamber and, even if plasma and cleaning gas are contacted with the inner wall, etching is less liable to occur and it is possible to extend the service life of the chamber. - FIGS. 13A and 13B each shows a practical structure of a
shower head 81 in this embodiment. - The
shower head 81 is comprised of a ring-type three-layered structure and so designed as to collect gases in the respective outer head sections into a middle-layer head section. That is, ring-like diffusion channels head sections diffusion channels head section 85 in one array to allow a corresponding gas to be discharged in a horizontal direction. For example, these discharge holes are so arranged as to allow different kinds of process gases to be sequentially discharged with an argon gas in between. - In the practical example shown in FIG. 13B, as a first combination the discharge holes85 b, 86 b, 85 b, 84 b, 85 b, 86 b, . . . , that is, an Ar gas, TiCl4 gas or ClF3 gas, Ar gas, NH3 gas, Ar gas, TiCl4 gas or ClF3 gas, . . . are used. As a second combination, the discharge holes 85 b, 86 b, 84 b, 85 b, 85 b, 86 b, 84 b, 85 b, , that is, the Ar gas, TiCl4 gas or ClF3, NH3 gas, Ar gas, Ar gas, TiCl4 gas or ClF3 gas, NH3 gas, Ar gas, . . . are used. It is needless to say that these combinations may be properly set depending upon the chamber configuration and process condition, etc. Further, to the TiCl4 gas and ClF3 gas, respective independent discharge holes may be provided.
- FIGS. 14A and 14B show a modified structure of the above-mentioned
shower head 81. Although, in the above-mentionedshower head 81, the gases from the respective head sections are collected into the middle layer head section, this modified structure is of such a type that a plurality of discharge holes are formed in the respective head sections in a not-overlapped fashion in a stacked direction. - This
shower head 90 is of a ring-type three-layered structure such that ring-like diffusion channels head sections diffusion channels - Various practical structures as shown in FIG. 15 are realized depending upon the order in which these head sections are stacked. In these structures, six cases are shown in FIG. 15. It is to be noted that the TiCl4 gas and ClF3 gas are switchingly used at a film forming time and cleaning time but that independent corresponding discharge holes may be provided for these gases.
- Even in these embodiments it is possible to obtain the same advantage as set out in connection with the above-mentioned embodiment.
- The shower heads for introducing the gases into the chamber can be variously changed or modified in the embodiment of the present invention.
- Although, in the above-mentioned embodiment, a plurality of members are used to introduced the process gas into the
chamber 11, as shown in FIG. 16, for example, a shower head is so configured as to have onegas introducing member 95 for allowing a process gas to be supplied from the top side of an upper bell jar onto a wafer W within a lower chamber and agas discharge section 96 connected to the lower end of thegas introducing member 95 and having a plurality of discharge holes to allow a gas to be spirally supplied down toward the wafer W. - As shown in FIG. 17, a shower head comprises one
gas introducing member 97 similar to thegas introducing member 95 and a plurality ofgas discharge sections 98 connected to the lower end of thegas introducing member 97, provided in an outwardly branched fashion and having a plurality of discharge holes so provided as to allow a gas to be discharged down onto a wafer W. Further, although two kinds of process gases are separately individually introduced into the chamber, these gases may be introduced together. - Although, in the above-mentioned respective embodiment, the formation of the TiN thin film has been explained, the present invention is not restricted thereto and other films may be formed. In the case where a film is formed using a Ti-containing material or Si-containing material, a Cl-containing gas is used as a feed gas and the present invention is effective to the formation of a film using these materials. As such materials, use is made of, for example, TiN, Ti, TiSiN, SiN, Ta, TaN, Ta2O5, PZT, BST, RuO and ZrO; a LOWK material, such as SiOF recently used as an insulating interlayer of a low dielectric constant; and Ta, TaN used as a barrier of Cu and SiN used as a etching stop.
- Although, in the above-mentioned embodiment, use is made of the ICP-CVD apparatus using a coil as an antenna, if the plasma CVD apparatus uses a chamber and bell jar, it can use a TCP (Transformer Coupled Plasma) using a spiral type antenna and it is also possible to use a helicon wave plasma processing apparatus using a helicon wave.
- Those applied forms of chambers provided in the processing apparatus according to the above-mentioned embodiments will be explained below with reference to FIGS. 18, 19 and20. As a lower chamber of the processing apparatus as will be explained below the
lower chamber 11 a shown in FIG. 1 is taken as an example and, as a gas supply system, a gas supply system for supplying a gas from the sidewall of the chamber shown in FIG. 12 is taken as an example. Here, only the featuring aspect is explained with the same reference numerals employed to designate corresponding parts or elements shown. And an explanation thereof is, therefore, omitted. - FIG. 18 is one example of a lower-height thin type chamber. This
thin type chamber 11 e is thin and has a height (depth) H of, for example, about 0.65 to 10 cm and, preferably, 0.65 to 5 cm. And the distance from the inner top surface of the chamber to a wafer W is about 3.8 to 30 cm and, preferably, 3.8 to 20 cm. Since, in this way, the chamber has a lower-volume shape, an exposed area within the chamber is smaller and hence the apparatus is smaller and ensures an easier maintenance. It is, therefore, possible to alleviate an evacuation load on thesystem 62. - An upper chamber11 f shown in FIG. 19 is of a semi-spherical type, that is, a bell jar type and an
upper chamber 11 g shown in FIG. 20 is of a dome-shaped type. According to these upper chambers, the distribution of an electric field by an antenna relative to the wafer W is made uniform compared with that of a box-type chamber and hence the thickness profile of a formed film, etching, etc., are made uniform. - FIG. 21 is a view showing a practical structure applied to a heat processing apparatus as a fifth embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
- The heat processing apparatus101 can perform an anneal process for promoting recrystallization of a formed film and a thermal oxidation process.
- This heat processing apparatus101 has a
susceptor 103 located within a chamber 102 to support a wafer W, awafer lifting mechanism 105 provided below thesusceptor 103 to allow the wafer W to be lifted up by a plurality of lift pins 104 at a transfer of the wafer W, aheater 106 provided in thesusceptor 103 and agas flow chamber 107 for hermetically supplying a gas such as an Ar gas and oxygen gas onto the wafer W. A sprayedfilm 14 of Al2O3/Y2O3 is formed on the inner surface of thegas flow chamber 107 and on the surface of aguide section 108 provided on thesusceptor 103 to guide a wafer mounting position and, by doing so, it is possible to obtain the same effect as in the above-mentioned respective embodiments. - FIG. 22 is a view showing a practical structure applied to an ashing apparatus as a sixth embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
- The ashing apparatus comprises a hermetically
sealable chamber 111 having a lower chamber 111 a andupper chamber 111 b, asusceptor 112 on which a wafer W is placed, aheater 113 provided in thesusceptor 112 to heat the wafer W, a gas supply system, not shown, for supplying a process gas such as oxygen, and an evacuation apparatus for evacuating the interior of thechamber 111. - In this ashing apparatus, a high-corrosion-resistant sprayed film is formed on the whole inner surface of the
upper chamber 111 band on the sidewall of the lower chamber 111 a except the inner bottom surface and, by doing so, it is possible to obtain the same effect as in the above-mentioned respective embodiment. - FIG. 23 is a view showing a practical structure applied to an etching apparatus as a seventh embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
- This etching apparatus comprises a hermetically
sealable chamber 121, a process gas supplying shower head provided within thechamber 121 and functioning as an upper electrode for plasma generation, asusceptor 123 allowing a wafer W to be placed and functioning as an upper electrode for plasma generation, a processgas supply system 126 having a plurality ofvalves 124 and a plurality ofprocess gas sources 125, a highfrequency power source 127 for applying a high frequency power to theshower head 122, ashield ring 128 provided around theshower head 122, anelectrostatic chuck system 129 provided on the top surface of thesusceptor 123, a focusingring 130 provided at an outer peripheral portion of theelectrostatic chuck 129 to surround the wafer W, agate valve 131 provided on the sidewall of thechamber 121 to allow the wafer to be loaded and unloaded into and out of thechamber 121, and adeposition shield 132 provided on the inner side surface of thechamber 121. - A sprayed
film 14 is formed, as the above-mentioned case, on exposed surfaces of thesusceptor 123, focusingring 130,shower head 122 andshield ring 128 within the chamber and further on the inner upper surface and inner bottom surface of thechamber 121. - It is to be noted that the sprayed film formed in the above-mentioned respective embodiments need only have a thickness of above 50 μm. In the case where the thickness of the sprayed film is less than 50 μm, the insulating resistance and withstand voltage are lower. This is based on our empirically obtained data showing a relation of a breakdown voltage to the film thickness shown in FIG. 24. According to FIG. 24, out of the film thickness range of 50 to 300 μm is preferable.
- Even in this embodiment, the same effect as set out in connection with the above-mentioned embodiment can be obtained by forming the sprayed film.
- Although, in the above-mentioned respective embodiments, the semiconductor wafer as a substrate has been explained by way of example, the present invention is not restricted thereto and it may also be applied to the formation of a glass substrate for a liquid crystal display device (LCD).
- According to the above-mentioned respective embodiments, a sprayed film of substantially Al2O3/Y2O3 whose weight ratio is above 0.5 is formed on the inner wall of the chamber and, by doing so, the chamber is less liable to be etched under a plasma and cleaning gas due to the presence of the high-corrosion resistant sprayed film. Thus the present invention can be preferably applied to the film formation, etching, ashing and heat treatment on a less-etching thermal sprayed film of the chamber.
- Further, since the gas supply system supplies a process gas near the upper zone of a wafer within the chamber, the gas hardly reaches the inner wall of the chamber and almost no product is deposited on the wall. As a material for the chamber, use can be made of a ceramic (Al2O3, SiO2, AlN, etc.), aluminum, stainless steel, metal or alloy.
- Additional advantages and modifications will readily occur to those skilled in the art. Therefore, the invention in its broader aspects is not limited to the specific details and representative embodiments shown and described herein. Accordingly, various modifications may be made without departing from the spirit or scope of the general inventive concept as defined by the appended claims and their equivalents.
Claims (27)
1. A processing apparatus comprising:
a chamber for holding a substrate that is to be processed;
a sprayed film formed on an inner surface of the chamber and containing a compound of a III-a element of the periodic table; and
a processing mechanism for processing a substrate held in the chamber.
2. The processing apparatus according to , wherein the sprayed film contains Al2O3.
claim 1
3. The processing apparatus according to , wherein the sprayed film comprises Al2O3 and Y2O3.
claim 1
4. The processing apparatus according to , wherein the weight ratio of Al2O3 to Y2O3 is 0.5 or more in the sprayed film.
claim 1
5. The processing apparatus according to , wherein a sprayed film containing a III-a element of the periodic table is formed on a part of the processing mechanism, which is exposed to the chamber.
claim 1
6. The processing apparatus according to , wherein the sprayed film is made of Y2O3, Sc2O3, Sc2F3, YF3, La2O3, CeO2, Eu2O3, or DyO3.
claim 1
7. The processing apparatus according to , wherein the sprayed film is made of Y2O3, Sc2O3, Sc2F3, YF3, La2O3, CeO2, Eu2O3, or DyO3.
claim 4
8. The processing apparatus according to , wherein the processing mechanism performs plasma process on the substrate.
claim 1
9. The processing apparatus according to , wherein the processing mechanism processes the substrate, while applying a corrosive gas into the chamber.
claim 1
10. The processing apparatus according to , wherein the processing mechanism performs a heating process on the substrate.
claim 1
11. A processing apparatus comprising:
a lower chamber containing a susceptor for holding a substrate that is to be processed;
an upper chamber provided above the lower chamber;
antenna means arranged around the upper chamber, for generating an induction magnetic field in the upper chamber and on the substrate;
high-frequency wave applying means for applying high-frequency power to the antenna means;
gas-supplying means for supplying a plurality of process gases onto the substrate in the lower chamber;
gas-exhausting means for exhausting the process gases from the upper and lower chambers; and
a film formed by sprayed on an inner surface of the upper chamber and containing a compound of a III-a element of the periodic table, for preventing corrosion from taking place while the substrate is being processed,
wherein an induction electromagnetic field is generated in the upper and lower chambers, generating a plasma, and the plasma is applied to the substrate, thereby to process the substrate.
12. A processing apparatus comprising:
a lower chamber containing a susceptor for holding a substrate that is to be processed;
an upper chamber provided above the lower chamber;
antenna means arranged around the upper chamber, for generating an induction magnetic field in the upper chamber and on the substrate;
high-frequency wave applying means for applying high-frequency power to the antenna means;
a gas-supplying means for shaped like a ring, surrounding an upper part of the lower chamber, and supplies the process gases and a plasma-generating gas into the lower chamber so that the gases may mix at a position above the substrate held on the susceptor; and
gas-exhausting means for exhausting the process gases from the upper and lower chambers,
wherein an induction electromagnetic field is generated in the upper chamber, generating a plasma, and the plasma is applied to the substrate, thereby to process the substrate.
13. The processing apparatus according to , wherein the gas-supplying means comprises a plurality of annular layers mounted one upon another, each having a gas-inlet port in the outer circumfrential surface and an inner passage connected to the gas-inlet port, one of the annular layers has a row of gas-outlet ports in the inner circumferential surface, every other gas-outlet port is connected to the inner passage of said one of the annular layers, and the remaining gas-outlet port are connected to the inner passages of the other annular layers alternately.
claim 9
14. The processing apparatus according to , wherein the gas-supplying means comprises a plurality of annular layers mounted one upon another, each having a gas-inlet port made in the outer circumfrential surface, an inner passage connected to the gas-inlet port, and a plurality of gas-outlet holes made in the inner circumferntial surface and connected to the inner passage, and the gas-outlet holes are arranged in staggered fashion in the inner circumferential surface of the gas-supplying means.
claim 9
15. The processing apparatus according to , wherein the sprayed film comprises an Al2O3 film and a Y2O3 film.
claim 8
16. The processing apparatus according to , wherein the weight ratio of the Al2O3 film to the Y2O3 film is 0.5 or more in the sprayed film.
claim 8
17. The processing apparatus according to , wherein the weight ratio of the Al2O3 film to the Y2O3 film is 0.5 or more in the sprayed film.
claim 2
18. The processing apparatus according to , wherein the weight ratio of the Al2O3 film to the Y2O3 film is 0.5 or more in the sprayed film.
claim 6
19. The processing apparatus according to , wherein the upper chamber has a base made of material selected from the group consisting of ceramic, metal, alloy containing the metal and hard plastic.
claim 8
20. The processing apparatus according to , wherein the ceramic is one selected from the group consisting of Al2O3, SiO2 and AlN.
claim 19
21. The processing apparatus according to , wherein the sprayed film has a thickness of 50 μm or more.
claim 8
22. The processing apparatus according to , which further comprises a coolant source for decreasing a temperature in the upper chamber, and in which the lower chamber and the upper chamber are connected in airtight fashion, the induction electromagnetic field generates a plasma above the susceptor, the gas-supplying means supplies process gases to the plasma, thereby forming a film on the substrate.
claim 8
23. The process apparatus according to , which further comprises a power supply for applying a high-frequency voltage between the lower and upper chambers, and in which the induction electromagnetic filed generates a plasma above the susceptor, the gas-supplying means supplies the process gases, and the high-frequency voltage is applied between the lower and upper chambers, thereby etching a surface of the substrate.
claim 8
24. The process apparatus according to , wherein the upper chamber is a semi-spherical one, a dome-shaped one, or a thin-type one shorter in height than a plasma-generating area.
claim 8
25. The process apparatus according to , wherein a weight ratio between Al2O3 to Y2O3 is 5:3 in the sprayed film.
claim 12
26. The process apparatus according to , wherein the film containing Y2O3 is YAG.
claim 21
27. The process apparatus according to , wherein the lower chamber is connected to the upper chamber and used as a heating chamber for performing heat processing on the substrate, an ashing chamber for removing a resist mask from the substrate or an etching chamber for etching the substrate.
claim 8
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/444,957 US7846291B2 (en) | 1999-12-10 | 2003-05-27 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
US11/980,570 US20080069966A1 (en) | 1999-12-10 | 2007-10-31 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
US11/980,596 US7879179B2 (en) | 1999-12-10 | 2007-10-31 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35201899 | 1999-12-10 | ||
JP11-352018 | 1999-12-10 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US10/444,957 Continuation US7846291B2 (en) | 1999-12-10 | 2003-05-27 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
Publications (1)
Publication Number | Publication Date |
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US20010003271A1 true US20010003271A1 (en) | 2001-06-14 |
Family
ID=18421226
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
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US09/731,722 Abandoned US20010003271A1 (en) | 1999-12-10 | 2000-12-08 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
US10/444,957 Expired - Fee Related US7846291B2 (en) | 1999-12-10 | 2003-05-27 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
US11/980,570 Abandoned US20080069966A1 (en) | 1999-12-10 | 2007-10-31 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
US11/980,596 Expired - Fee Related US7879179B2 (en) | 1999-12-10 | 2007-10-31 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
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US10/444,957 Expired - Fee Related US7846291B2 (en) | 1999-12-10 | 2003-05-27 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
US11/980,570 Abandoned US20080069966A1 (en) | 1999-12-10 | 2007-10-31 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
US11/980,596 Expired - Fee Related US7879179B2 (en) | 1999-12-10 | 2007-10-31 | Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film |
Country Status (4)
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US (4) | US20010003271A1 (en) |
JP (4) | JP2001226773A (en) |
KR (15) | KR20010062209A (en) |
TW (1) | TW514996B (en) |
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