TWI833804B - 含鋁膜的間隙填充 - Google Patents
含鋁膜的間隙填充 Download PDFInfo
- Publication number
- TWI833804B TWI833804B TW108133158A TW108133158A TWI833804B TW I833804 B TWI833804 B TW I833804B TW 108133158 A TW108133158 A TW 108133158A TW 108133158 A TW108133158 A TW 108133158A TW I833804 B TWI833804 B TW I833804B
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- Taiwan
- Prior art keywords
- aluminum
- feature
- film
- substrate surface
- substrate
- Prior art date
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- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 74
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 68
- 239000000758 substrate Substances 0.000 claims abstract description 169
- 238000000034 method Methods 0.000 claims abstract description 168
- 239000002243 precursor Substances 0.000 claims abstract description 42
- 238000000151 deposition Methods 0.000 claims abstract description 36
- 239000012025 fluorinating agent Substances 0.000 claims abstract description 20
- 239000000376 reactant Substances 0.000 claims abstract description 17
- 238000012545 processing Methods 0.000 claims description 56
- 238000005530 etching Methods 0.000 claims description 27
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 claims description 27
- 238000003672 processing method Methods 0.000 claims description 17
- 238000011282 treatment Methods 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000007800 oxidant agent Substances 0.000 claims description 8
- 239000003153 chemical reaction reagent Substances 0.000 claims description 7
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 6
- -1 aluminum alkoxide Chemical class 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 4
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- 239000003446 ligand Substances 0.000 claims description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 3
- 229910019800 NbF 5 Inorganic materials 0.000 claims description 3
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 claims description 3
- 229910001507 metal halide Inorganic materials 0.000 claims description 3
- 150000005309 metal halides Chemical class 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 125000005234 alkyl aluminium group Chemical group 0.000 claims description 2
- QAMFBRUWYYMMGJ-UHFFFAOYSA-N hexafluoroacetylacetone Chemical compound FC(F)(F)C(=O)CC(=O)C(F)(F)F QAMFBRUWYYMMGJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000007789 gas Substances 0.000 description 132
- 239000010408 film Substances 0.000 description 70
- 238000009826 distribution Methods 0.000 description 39
- 230000008021 deposition Effects 0.000 description 25
- 238000000231 atomic layer deposition Methods 0.000 description 22
- 235000012431 wafers Nutrition 0.000 description 21
- 239000003570 air Substances 0.000 description 20
- 238000003682 fluorination reaction Methods 0.000 description 17
- 239000010410 layer Substances 0.000 description 13
- 238000010926 purge Methods 0.000 description 13
- 238000000429 assembly Methods 0.000 description 10
- 230000000712 assembly Effects 0.000 description 10
- 238000011049 filling Methods 0.000 description 10
- 239000011261 inert gas Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 9
- 230000002093 peripheral effect Effects 0.000 description 9
- 238000012546 transfer Methods 0.000 description 9
- 238000010586 diagram Methods 0.000 description 7
- 238000005229 chemical vapour deposition Methods 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminium flouride Chemical compound F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 5
- 230000006870 function Effects 0.000 description 5
- 238000011068 loading method Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910018085 Al-F Inorganic materials 0.000 description 4
- 229910018179 Al—F Inorganic materials 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910016569 AlF 3 Inorganic materials 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 238000010574 gas phase reaction Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000001878 scanning electron micrograph Methods 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- 229910018516 Al—O Inorganic materials 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000000137 annealing Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000000059 patterning Methods 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- IRPGOXJVTQTAAN-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanal Chemical compound FC(F)(F)C(F)(F)C=O IRPGOXJVTQTAAN-UHFFFAOYSA-N 0.000 description 1
- 101100058670 Aeromonas hydrophila subsp. hydrophila (strain ATCC 7966 / DSM 30187 / BCRC 13018 / CCUG 14551 / JCM 1027 / KCTC 2358 / NCIMB 9240 / NCTC 8049) bsr gene Proteins 0.000 description 1
- 229910017077 AlFx Inorganic materials 0.000 description 1
- 229910017109 AlON Inorganic materials 0.000 description 1
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 230000033444 hydroxylation Effects 0.000 description 1
- 238000005805 hydroxylation reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009616 inductively coupled plasma Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000004377 microelectronic Methods 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 231100000812 repeated exposure Toxicity 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 230000037351 starvation Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
- H01L21/28506—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers
- H01L21/28512—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table
- H01L21/28556—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table by chemical means, e.g. CVD, LPCVD, PECVD, laser CVD
- H01L21/28562—Selective deposition
-
- 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
- C23C16/22—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 deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
- C23C16/301—AIII BV compounds, where A is Al, Ga, In or Tl and B is N, P, As, Sb or Bi
- C23C16/303—Nitrides
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76877—Filling of holes, grooves or trenches, e.g. vias, with conductive material
-
- 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
- C23C16/04—Coating on selected surface areas, e.g. using masks
- C23C16/045—Coating cavities or hollow spaces, e.g. interior of tubes; Infiltration of porous substrates
-
- 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
- C23C16/22—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 deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
- C23C16/32—Carbides
-
- 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
- C23C16/45519—Inert gas curtains
-
- 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
- C23C16/45523—Pulsed gas flow or change of composition over time
- C23C16/45525—Atomic layer deposition [ALD]
- C23C16/45527—Atomic layer deposition [ALD] characterized by the ALD cycle, e.g. different flows or temperatures during half-reactions, unusual pulsing sequence, use of precursor mixtures or auxiliary reactants or activations
- C23C16/45534—Use of auxiliary reactants other than used for contributing to the composition of the main film, e.g. catalysts, activators or scavengers
-
- 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
- C23C16/45523—Pulsed gas flow or change of composition over time
- C23C16/45525—Atomic layer deposition [ALD]
- C23C16/45527—Atomic layer deposition [ALD] characterized by the ALD cycle, e.g. different flows or temperatures during half-reactions, unusual pulsing sequence, use of precursor mixtures or auxiliary reactants or activations
- C23C16/45536—Use of plasma, radiation or electromagnetic fields
-
- 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
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Abstract
沉積膜的方法包括在基板表面的特徵中以自下而上方式沉積含鋁間隙-填充膜。基板可連續多次暴露於含鋁前驅物、反應物、氟化劑和蝕刻劑中,以促進特徵中膜的自下而上生長。
Description
本申請主張於2018年9月21日提交的美國臨時申請號62/734,625的優先權,其全部揭露內容藉由引用合併於此。
本揭露內容總體涉及沉積薄膜的方法。特別地,本揭露內容涉及用於填充窄溝槽的間隙填充製程。
在微電子元件製造中,需要填充深寬比(AR)為大約5:1或更大的窄溝槽且沒有空隙以用於很多應用中。一種應用是圖案化。其他應用包括但不限於:記憶體電容器(DRAM、快閃記憶體、ReRAM、MIM電容器)、用於控制開關門(電晶體)的介電膜、光學功能膜(光學隔離)和支撐電路結構的機械膜(虛擬閘極)。
與典型的介電膜(諸如SiO、SiN、SiCN和Si)相比,氧化鋁和其他鋁基膜(例如氮化鋁)的乾蝕刻速率低。
需要一種利用鋁基膜進行間隙填充的方法,從而導致自下而上膜的生長,其中剛沉積的膜是高質量的,具有最小化空隙至無空隙。
本揭露內容的一個或多個實施例針對一種包括在基板表面的特徵中沉積含鋁間隙-填充膜的處理方法,特徵延伸的深度從基板表面至底面,至少一個特徵具有由第一側壁和第二側壁界定的寬度。以自下而上方式沉積膜。
本揭露內容的額外實施例涉及一種處理方法,該處理方法包括:將基板表面定位在製程腔室中。基板表面上具有至少一個特徵。至少一個特徵產生具有底部、頂部與側壁的間隙。基板表面暴露於含鋁前驅物和反應物,從而在基板表面上形成共形的含鋁膜。使基板表面暴露於氟化劑和蝕刻劑,以相對於特徵的底部優先蝕刻特徵頂部的共形含鋁膜。優先蝕刻後,可選擇性地將基板表面暴露於氧化劑。依次暴露於前驅物和反應物,然後暴露於氟化劑和蝕刻劑以及可選的氧化劑,以自下而上方式填充特徵的間隙。
揭露內容的其他實施例針對於處理方法,包括:將具有基板表面的基板放入包括多個部分的製程腔室中,每個部分由氣簾與相鄰部分隔開,基板表面具有至少一個特徵,至少一個特徵具有頂部、底部和側面,且深寬比大於或等於10:1。基板表面的至少一部分在製程腔室的第一部分中暴露於第一製程條件,第一製程條件包括含鋁前驅物。基板表面橫向移動通過氣簾到製程腔室的第二部分。基板表面在製程腔室的第二部分中暴露於第二製程條件,第二製程條件包含與含鋁前驅物形成膜的反應物,膜包含根據AlCx
Oy
Nz
的物質,其中x、y和z獨立地在0-3的範圍內。基板表面橫向移動通過氣簾到製程腔室的第三部分。基板表面在製程腔室的第三部分中暴露於第三製程條件,第三製程條件包含氟化劑。基板表面移動通過氣簾到製程腔室的第四部分。基板表面在製程腔室的第四部分中暴露於第四製程條件,第四製程條件包括蝕刻劑。基板表面可選擇性地移動通過氣簾到製程腔室的第五部分。基板表面可選性地在製程腔室的第五部分中暴露於第五製程條件,第五製程條件包含氧化劑。包括基板表面的橫向移動的重複暴露於第一部分、第二部分、第三部分、第四部分以及可選的第五部分以填充特徵。
在描述揭露內容的幾個示例性實施例之前,應當理解,揭露內容不限於在以下描述中闡述的構造或製程步驟的細節。揭露內容能夠用於其他實施例,並且能夠以各種方式來實踐或執行。
本文所用之「基板」是指在製造製程中在其上進行膜處理的任何基板或基板上形成的材料表面。舉例而言,上方可進行處理的基板表面包括諸如下列的材料:取決於應用的矽、氧化矽、應變矽、絕緣體上矽(SOI)、碳摻雜的氧化矽、非晶矽、摻雜矽、鍺、砷化鎵、玻璃、藍寶石以及任何其他材料,例如金屬、金屬氮化物、金屬合金和其他導電材料。基板包括但不限於半導體晶片。可將基板暴露於預處理製程,以拋光、蝕刻、還原、氧化、羥基化、退火和/或烘烤基板表面。除了直接在基板本身的表面上進行膜處理外,在本揭露內容中,所揭露的任何膜處理步驟還可在形成於基板上的底層上進行,如以下更詳細地揭露,而術語「基板表面」旨在包括上下文指示的上述底層。因此,舉例而言,在已將膜/層或部分膜/層沉積到基板表面上的情況下,新沉積的膜/層的暴露表面成為基板表面。
氧化鋁(AlO)用於圖案化應用。與典型的介電膜(例如SiO、SiN、SiCN和Si)相比,AlO具有較低的乾蝕刻速度。因此,為了自下而上間隙-填充基板的特徵,AlO與其他膜相比具有良好的蝕刻選擇性。除了AlO之外,合適的間隙填充膜包括以下物質,這些物質包括但不限於:AlN、AlC、AlCN、金屬Al等,通常稱為AlCx
Oy
Nz
,其中,x、y和z根據原子種類的性質獨立地在0-3的範圍內。如本領域技術人員將理解的,其中x、y和z獨立地在0-1的範圍內的AlCx
Oy
Nz
並非是化學計量的,而是代表原子組成。舉例而言,化學計量膜Al2
O3
可以稱為AlC0
O1.5
N0
。上述膜也可以用原子組成而非化學計量來稱呼–如碳化鋁、氧化鋁、氮化鋁、碳氧化鋁、氮氧化鋁、碳氮化鋁和/或碳氮氧化鋁。
揭露內容的一個或多個實施例涉及一種處理方法,包括在基板上的特徵中以自下而上方式沉積含鋁間隙-填充膜。就此而言,術語「自下而上方式」是指膜相對於特徵的頂部優先沉積在特徵的底部。本文的方法針對非保形蝕刻,其中特徵頂部的蝕刻速度高於特徵底部的蝕刻速度。
揭露內容的一個或多個實施例涉及相對於特徵的底部優先蝕刻特徵的頂部的方法,隨後是膜沉積,以便以自下而上的方式生長膜。揭露內容的某些實施例提供了有利地以膜填充大於5:1或甚至10:1的深寬比的特徵的方法。揭露內容的一個或多個實施例有利地提供了具有高產量和可重複性的間隙填充特徵的方法。
根據一個或多個實施例,方法使用化學氣相沉積(CVD)製程。在上述實施例中,基板表面同時暴露於第一反應性氣體和第二反應性氣體,以使第一反應性氣體和第二反應性氣體在膜的形成過程中混合。
根據一個或多個實施例,方法使用原子層沉積(ALD)製程。在上述實施例中,基板表面依序或基本上依序暴露於前驅物(或反應性氣體)。在整個說明書中,「基本上依序」是指前驅物暴露的大部分時間與共同反應物的暴露不重疊,儘管可能存在一些重疊。如本說明書和所附申請專利範圍中所使用的術語「前驅物」、「反應物」、「反應性氣體」等可互換使用,以代表可與基板表面反應的任何氣態物質,或基板表面上存在的物質。
在一個或多個實施例中,使用原子層沉積(ALD)製程進行間隙-填充方法。ALD製程是一種自我限制製程,其中使用二元(或更高階)反應沉積單層材料。理論上,單個ALD反應是自我限制,直到基板表面上所有可用的活性位點都發生反應為止。可以通過時域或空間ALD來執行ALD製程。
在時域製程中,製程腔室和基板在任何給定時間暴露於單一反應性氣體。在示例性時域製程中,可以在製程腔室中填充金屬前驅物一段時間,以使金屬前驅物與基板上的可用位點完全反應。然後可以清除製程腔室中的前驅物,然後再將第二種反應性氣體流入製程腔室中,並使第二種反應性氣體與基板表面或基板表面上的材料充分反應。時域製程通過確保在任何給定時間在製程腔室中僅存在一種反應性氣體來最小化反應性氣體的混合。在任何反應性氣體暴露開始時,都會有一個延遲,其中反應性物種的濃度從零增加到最終的預定壓力。同樣,從製程腔室清除所有反應性物種也存在延遲。
在空間ALD製程中,基板在單個製程腔室內的不同製程區域之間移動。每個單獨的製程區域都通過氣簾與相鄰的製程區域分開。氣簾有助於防止反應性氣體混合,從而最小化任何氣相反應。基板移動通過不同的製程區域允許基板順序地暴露於不同的反應性氣體,同時防止氣相反應。
揭露內容的某些實施例是針對使用批次製程腔室(也稱為空間製程腔室)的膜沉積製程。圖1示出了包括氣體分配組件120(也稱為注射器或注射器組件)和基座組件140的製程腔室100的橫剖面。氣體分配組件120是在製程腔室中使用的任何類型的氣體輸送元件。氣體分配組件120包括面對基座組件140的前表面121。前表面121可具有任意數量或種類的開口,以輸送氣體流朝向基座組件140。氣體分配組件120還包括外邊緣124,外邊緣124在所示的實施例中基本上是圓形的。
所使用的氣體分配組件120的具體類型可能取決於所使用的特定製程會有所不同。揭露內容的實施例可以與控制基座和氣體分配組件之間的間隙的任何類型的處理系統一起使用。在二元反應中,複數個氣體通道可包括至少一個第一反應性氣體A通道、至少一個第二反應性氣體B通道、至少一個淨化氣體P通道和/或至少一個真空V通道。從第一反應性氣體A通道、第二反應性氣體B通道和淨化氣體P通道流出的氣體被引向晶圓的頂表面。一些氣流在水平方向上移動橫跨晶圓的表面,並通過淨化氣體P通道離開處理區域。
在某些實施例中,氣體分配組件120是由單個注射器單元製成的剛性固定主體。在一個或多個實施例中,氣體分配組件120由複數個單獨的扇區(例如,注射器單元122)組成,如圖2所示。單件主體或多扇區主體均可與所描述的揭露內容的各種實施例一起使用。
基座組件140位於氣體分配組件120下方。基座組件140包括頂表面141與頂表面141中的至少一個凹部142。基座組件140還具有底面143與邊緣144。凹部142可以是任何合適的形狀和尺寸,這取決於被處理的基板60的形狀和尺寸。在圖1所示的實施例中,凹部142具有平坦的底部以支撐晶圓的底部;但是,凹部的底部可能會有所不同。在某些實施例中,凹部在凹部的外圍邊緣周圍有台階區域,其大小適合於支撐晶圓的外圍邊緣。台階所支撐的晶圓的外周邊緣的量可以根據例如晶圓的厚度和在晶圓的背面已經存在的特徵而變化。
在某些實施例中,如圖1所示,基座組件140的頂表面141中的凹部142經調整尺寸,使得支撐在凹部142中的基板60具有與基座140的頂表面141基本上共面的頂表面61。如本說明書和所附申請專利範圍中所使用的,術語「基本上共面」是指晶圓的頂表面和基座組件的頂表面共面在±0.2mm以內。在某些實施例中,頂表面共面在± 0.15 mm以內、± 0.10 mm以內或± 0.05 mm以內。
圖1的基座組件140包括能夠提升、降低和旋轉基座組件140的支撐柱160。基座組件在支撐柱160的中心內可包括加熱器、或氣體線路或電氣部件。支撐柱160可能是增加或減小基座組件140和氣體分配組件120之間的間隙,將基座組件140移動到適當位置的主要方法。基座組件140還可包括微調致動器162,微調致動器162可對基座組件140進行微調整,以在基座組件140和氣體分配組件120之間產生預定的間隙170。
在某些實施例中,間隙170距離在約0.1 mm至約5.0 mm範圍中、或約0.1 mm至約3.0 mm範圍中、或約0.1 mm至約2.0 mm範圍中、或約0.2 mm至約1.8 mm範圍中、或約0.3 mm至約1.7 mm範圍中、或約0.4 mm至約1.6 mm範圍中、或約0.5 mm至約1.5 mm範圍中、或約0.6 mm至約1.4 mm範圍中、或約0.7 mm至約1.3 mm範圍中、或約0.8 mm至約1.2 mm範圍中、或約0.9 mm至約1.1 mm範圍中或為約1 mm。
圖中所示的製程腔室100是轉盤式腔室,其中基座組件140可容納複數個基板60。如圖2所示,氣體分配組件120可包括複數個分開的注射器單元122,每個注射器單元122能夠在晶圓在注射器單元下方移動時將膜沉積在晶圓上。示出了兩個扇形注射器單元122,兩個扇形注射器單元122定位在基座組件140的大約相反的兩側上和上方。所示注射器單元122的數量僅出於示例性目的。將理解的是,可以包括更多或更少的注射器單元122。在某些實施例中,有足夠數量的扇形注射器單元122形成與基座組件140的形狀相符的形狀。在某些實施例中,每個單獨的扇形注射器單元122中可獨立地移動、移除和/或更換,而不影響任何其他注射器單元122。舉例而言,可抬起一個片段以允許機器人進入基座組件140和氣體分配組件120之間的區域以加載/卸載基板60。
具有多個氣體注射器的製程腔室可用於同時處理多個晶圓,從而使晶圓經歷相同的製程流程。舉例而言,如圖3中所示,製程腔室100具有四個氣體注射器組件和四個基板60。在處理開始時,可將基板60放置在注射器組件30之間。旋轉17基座組件140 45º,將使位於氣體分配組件120之間的每個基板60移動到用於膜沉積的氣體分配組件120,如氣體分配組件120下的虛線圓形所示。額外的45º旋轉將使基板60遠離注射器組件30。基板60和氣體分配組件120的數量可以相同或不同。在某些實施例中,所處理的晶圓數量與氣體分配組件的數量相同。在一個或多個實施例中,被處理的晶圓數量是氣體分配組件數量的分數或整數倍。舉例而言,如果有四個氣體分配組件,則有4x個晶圓接受處理,其中x是大於或等於1的整數。在示例性實施例中,氣體分配組件120包括由氣簾隔開的八個處理區域,而基座組件140可容納六個晶圓。
圖3中所示的製程腔室100僅表示一種可能的配置,並且不應被視為限制本揭露內容的範圍。在此,製程腔室100包括複數個氣體分配組件120。在所示的實施例中,有四個氣體分配組件(也稱為注射器組件30)圍繞製程腔室100均勻地間隔開。製程腔室100所示為八角形;然而,本領域技術人員將理解,這是一種可能的形狀,並且不應被視為限制本揭露內容的範圍。所示的氣體分配組件120是梯形的,但也可以是單個圓形部件,或者也可以如圖2所示般由多個扇形段組成。
圖3所示的實施例包括一個裝載閘腔室180,或一個像緩衝站的輔助腔室。此腔室180連接至製程腔室100的一側,以允許例如從腔室100裝載/卸載基板(也稱為基板60)。晶圓機器人可放置在腔室180中,以將基板移動到基座上。
轉盤(例如基座組件140)的旋轉可以是連續的也可以是間歇的(不連續的)。在連續處理中,晶圓不斷旋轉,以使它們依次暴露於每個注射器。在不連續處理中,晶圓可被移動到注射器區域並停止,然後移至注射器之間的區域84並停止。舉例而言,轉盤可以旋轉,從而使晶圓從注射器間的區域移動穿過注射器(或在注射器附近停止),然後移動到下一個注射器間的區域,在該區域中,轉盤可以再次暫停。注射器之間的暫停可能會為每個層沉積之間的額外處理(例如暴露於電漿)提供時間。
圖4示出了氣體分配組件220的扇區或部分,其可以被稱為注射器單元122。注射器單元122可以單獨使用或與其他注射器單元組合使用。舉例而言,如圖5所示,四個圖4的注射器單元122被組合以形成單個氣體分配組件220。(為了清楚起見,未將分隔四個注射器單元的線顯示。)儘管圖4的注射器單元122除了具有淨化氣體通口155和真空通口145之外還具有第一反應性氣體通口125和第二氣體通口135,但是注射器單元122不需要所有這些部件。
參照圖4和圖5兩者,根據一個或多個實施例的氣體分配組件220可包括複數個扇區(或注射器單元122),每個扇區相同或不同。氣體分配組件220位於製程腔室內,並且在氣體分配組件220的前表面121中包括複數個細長的氣體通口125、135、155和細長的真空通口145。複數個細長的氣體通口125、135、155和細長的真空通口145從鄰近氣體分配組件220的內周邊緣123的區域向鄰近氣體分配組件220的外周邊緣124的區域延伸。所示的複數個氣體通口包括第一反應性氣體通口125、第二氣體通口135、圍繞第一反應性氣體通口和第二反應性氣體通口中的每一個的真空通口145、和淨化氣體通口155。
參照圖4或圖5所示的實施例,當說明通口從至少內周邊區域附近延伸到至少外周邊區域附近時,通口可不僅僅是從內到外徑向延伸。當真空通口145圍繞反應性氣體通口125和反應性氣體通口135時,通口可切向延伸。在圖4和5所示的實施例中,楔形反應性氣體通口125、135在所有邊緣上被真空通口145包圍,包括鄰近內周邊區域和外周邊區域。
參照圖4,隨著基板沿著路徑127移動,基板表面的每個部分都暴露於多種反應性氣體。為了沿著路徑127,基板將暴露於或「看到」淨化氣體通口155、真空通口145、第一反應性氣體通口125、真空通口145、淨化氣體通口155、真空通口145、第二氣體通口135與真空通口145。因此,在圖4中所示的路徑127的末端,基板已經暴露於第一氣體通口125和第二氣體通口135以形成層。所示的注射器單元122成四分之一圈,但可以更大或更小。圖5中所示的氣體分配組件220可以視為四個圖4中的注射器單元122串聯連接的組合。
圖4的注射器單元122示出了將反應性氣體分開的氣簾150。術語「氣簾」用於描述分開反應性氣體以避免混合的氣流或真空的任何組合。圖4所示的氣簾150包括真空通口145的靠近第一反應性氣體通口125的部分,在中間的淨化氣體通口155,和真空通口145的靠近第二氣體通口135的部分。氣流和真空的這種組合可用於防止或最小化第一反應性氣體和第二反應性氣體的氣相反應。
參照圖5,來自氣體分配組件220的氣流和真空的組合形成分離成複數個處理區域250。圍繞單個氣體通口125、135大致定義處理區域250,氣簾150位於處理區域250之間。圖5所示的實施例構成了八個分開的處理區域250,它們之間具有八個分別的氣簾150。製程腔室可具有至少兩個處理區域。在某些實施例中,至少有三個、四個、五個、六個、七個、八個、九個、10個、11個或12個處理區域。
在處理期間,基板可在任何給定時間暴露於一個以上的處理區域250。但是,暴露於不同處理區域的部分將具有將兩者分開的氣簾。舉例而言,如果基板的前邊緣進入包括第二氣體通口135的處理區域,則基板的中間部分將位於氣簾150的下方,基板的尾部邊緣將位於包括第一反應性氣體通口125的處理區域中。
工廠接口280,例如可以是裝載閘腔室,被示為連接到製程腔室100。基板60被示為疊加在氣體分配組件220上以提供參考框架。基板60通常可坐在要固定在氣體分配組件120的前表面121附近的基座組件上。基板60通過工廠接口280被加載到製程腔室100中到基板支撐件或基座組件上(參見圖3)。可將基板60示出為位於處理區域內,因為基板位於第一反應性氣體通口125附近並且在兩個氣簾150a、150b之間。沿路徑127旋轉基板60將使基板沿製程腔室100逆時針移動。因此,基板60將暴露於第一處理區域250a至第八處理區域250h,包括介於第一處理區域250a與第八處理區域250h之間的所有處理區域。
揭露內容的實施例涉及的處理方法包括具有複數個處理區域250a-250h的製程腔室100,其中每個處理區域通過氣簾150與相鄰區域分開。舉例而言,圖5中所示的製程腔室。製程腔室內的氣簾和處理區域的數量可以是任意合適的數量,具體取決於氣流的佈置。圖5所示的實施例具有八個氣簾150和八個處理區域250a-250h。氣簾的數量通常等於或大於處理區域的數量。
複數個基板60位於基板支撐件上,基板支撐件例如圖1與圖2所示的基板組件140。複數個基板60圍繞處理區域旋轉以進行處理。通常,在整個處理期間,包括沒有反應性氣體流入腔室的期間,氣簾150處於接合狀態(氣體流動並處於真空狀態)。
第一反應性氣體A流入一個或多個處理區域250,而惰性氣體則流入沒有第一反應性氣體A流入的任何處理區域250。舉例而言,如果第一反應性氣體流入處理區域250b至處理區域250h,則惰性氣體將流入處理區域250a。惰性氣體可流過第一反應性氣體通口125或第二氣體通口135。
處理區域內的惰性氣體可以是恆定的也可以是變化的。在某些實施例中,反應性氣體與惰性氣體共流。惰性氣體將充當載體和稀釋劑。由於反應性氣體相對於載氣的量較小,因此共流可通過減小相鄰區域之間的壓力差來使處理區域之間的氣體壓力平衡更加容易。
圖6顯示了帶有特徵310的基板60的局部橫剖視圖。為了說明目的,這些圖示出了具有單個特徵的基板;然而,本領域技術人員將理解可以有多個特徵。特徵310的形狀或剖面可以是任何合適的形狀或剖面,包括但不限於(a)垂直側壁與底面、(b)錐形側壁、(c)底切、(d)凹入剖面、(e)彎曲、(f)微溝槽、(g)彎曲底面和(h)切口。就此而言,術語「特徵」是指任何故意的表面不規則性。特徵的合適實施例包括但不限於具有頂部、兩個側壁和底部的溝槽和孔,具有頂部和兩個側壁的峰。特徵可具有任何合適的深寬比(特徵深度與特徵寬度的比)。在某些實施例中,深寬比大於或等於約5:1、10:1、15:1、20:1、25:1、30:1、35:1或40:1。
基板60具有基板表面320。至少一個特徵310在基板表面320中形成開口。特徵310從基板表面320延伸到深度D到底面312。特徵310具有界定特徵310的寬度W的第一側壁314和第二側壁316。由側壁和底部形成的開口區域也稱為間隙。
圖7示出了根據本揭露內容的一個或多個實施例的含鋁膜的自下而上間隙-填充製程的製程400流程圖。參照圖7與圖8A至圖8E,在410為處理提供了基板60。就此而言,術語「提供」是指將基板放置在用於進一步處理的位置或環境中。在420處,將含Al膜330沉積在基板表面320以及特徵310的側壁314、316和底部312上。含Al膜330的形成包括依序地將基板表面暴露於含鋁前驅物和反應物。可以根據需要在直接連續步驟422中重複進行沉積420。此外,在使用蝕刻劑440之後重複沉積420,直到形成間隙填充膜。在一個或多個實施例中,填充特徵的深度和寬度被且沒有空隙或接縫。根據一個或多個實施例,含鋁間隙-填充膜的厚度範圍為約10 Å至約10000 Å。
形成的膜可以是任何合適的膜。在某些實施例中,形成的膜是包含根據AlCx
Oy
Nz
(I)的一或多個物種的非晶或結晶含鋁膜,其中x、y和z根據原子物種的性質獨立地在0-3的範圍內,其中該式代表原子組成,而不是化學計量的。此式包括:AlO、AlN、AlC、AlON、AlOC、AlCN、AlOCN、金屬Al等等。膜可由下列任何合適的製程形成,包括但不限於化學氣相沉積(CVD)、電漿輔助化學氣相沉積(PECVD)、原子層沉積(ALD)與電漿輔助原子層沉積(PEALD)。鋁的前驅物可以是任何揮發性鋁源。合適的鋁前驅物包括但不限於AlR3
,其中R=通過C、N、O、H、S或鹵化物與Al結合的任何配體。舉例而言,鋁前驅物可包括下列一或多者:含烷基鋁化合物、基於烷氧化鋁的化合物、基於鋁氨基的化合物、鋁鹵化物或上述之組合。在實施例中,鋁前驅物是三甲基鋁(TMA)。可在熱罐中加熱前驅物以增加蒸氣壓,並使用載氣(例如,超高純(UHP)Ar、He、H2
、N2
等)將其送入腔室。反應物可包括氧源、氮源、碳源、氫源或上述之組合。反應物可選自下列所構成之群組:O2
、O2
電漿、NO、NO電漿、N2
O、N2
O電漿、H2
O、H2
O電漿、D2
O、O3
、NH3
、NH3
電漿、N2
、N2
電漿、肼、CO2
、C1
-C6
碳氫化合物、H2
、H2
電漿、甲醇、乙醇、異丙醇、或Al-前驅物。
在某些實施例中,膜330在至少一個特徵上共形地形成。如本文所用,術語「共形」或「共形地」是指黏附並均勻覆蓋暴露表面的層的厚度相對於膜的平均厚度的變化小於5%。舉例而言,1,000 Å厚膜在厚度中將具有小於50 Å的變化。此厚度與變化包括凹部的邊緣、角落、側面和底部。舉例而言,在揭露內容的各種實施例中,由ALD沉積的共形層將在複合物表面上沉積區域上提供基本均勻厚度的覆蓋。
在某些實施例中,膜330是連續膜。如本文所用,術語「連續」是指覆蓋整個暴露表面而沒有間隙或裸露點的層,所述間隙或裸露點暴露沉積層下面的材料。連續層可具有表面面積小於膜總表面面積的約1%的間隙或裸點。
取決於例如所使用的前驅物,沉積420期間的溫度可以是任何合適的溫度。在某些實施例中,沉積溫度在約50 ℃至550 ℃的範圍中、或約200 ℃至約500 ℃的範圍中或約250 ℃至約450 ℃的範圍中。沉積420可以在有或沒有電漿的情況下發生。電漿可以是電容耦合電漿(CCP)或電感耦合電漿(ICP)或微波,也可以是直接電漿或遠端電漿。沉積420過程的製程腔室壓力可在約50毫托至750托的範圍中、或約100毫托至約400托的範圍中、或約1托至約100托的範圍中、或約6.5托至約30托的範圍中。
通常,僅氟源對蝕刻含鋁膜無效。因此,本文揭露的蝕刻製程包括:氟化和蝕刻劑的使用。此製程導致非共形蝕刻,其中特徵(例如,溝槽)頂部的蝕刻速度大於特徵底部的蝕刻速度。氟化430用氟化物源(也稱為氟化劑)處理含Al膜(AlCx
Oy
Nz
;x、y和z獨立地在0-3的範圍內)。氟化劑的反應性應足以將AlCx
Oy
Nz
轉化為AlF3
。氟化劑可包括電漿。電漿可為指向性電漿。氟化劑可包括WF6
、NF3
電漿、NbF5
、XeF2
、F2
、TiF4
、氟化氫(HF)、吡啶-HF、烷基胺-HF、金屬鹵化物、或上述之組合。在實施例中,氟化劑包括:WF6
、NF3
電漿、NbF5
、XeF2
、F2
、TiF4
、烷基胺-HF、金屬鹵化物、HF、或上述之組合。
根據某些實施例,通過將特徵暴露於電漿氟化方法(例如NF3
電漿)中,可誘使特徵的頂部比底部具有更高的氟化度。由於電漿固有地由於離子的存在而具有方向性,因此當將深寬比為10:1或更大的結構暴露於電漿時,不希望受到理論的束縛,可以預期在特徵的頂部比底部具有更高的氟化度。同樣地,相對於特徵的底部優選氟化特徵的頂部(例如,使用氟化前驅物飢餓)可促進非共形氟化,從而在使用蝕刻劑440造成整體非共形蝕刻。如果有更多的AlF3
,只要基板被蝕刻劑浸透,頂部的蝕刻度應高於底部的蝕刻度。
在某些實施例中,非共形蝕刻(或非共形氟化)是通過熱氟化方法(無電漿)誘導的,其中控制氟化分子的濃度,使得與底部相比,溝槽頂部的氟化分子更多,從而導致頂部的氟化更多,蝕刻速度更高。在另一態樣中,氟化的量也可由基板溫度確定(溫度越高,氟化越多)。含Al膜330的氟化包括將基板表面暴露於氟化劑,這形成如圖8B所示的氟化部分340。氟化部分包括AlF3
。
使用蝕刻劑440從表面去除AlF3
。用蝕刻劑飽和有助於去除剩餘的Al-F鍵。可將蝕刻劑定義為可以與AlF3
反應以形成從表面去除揮發性AlF物質的任何化合物。蝕刻劑可以是在表面上將某種類型的配體(L)轉移至Al並形成揮發性Ln
AlFm
物種的分子。非限制性實施例包括三甲基鋁(TMA)與Sn(acac)2
。鋁烷基與某些Sn(II)化合物亦可用作為蝕刻劑。在一個或多個實施例中,蝕刻劑可包括下列的一者或多者:R’3
Al,其中R’是烷基、胺或上述之組合,例如三甲基鋁(TMA);Sn(R’’)2
,其中R’’是乙醯丙酮(acac)、六氟乙醯丙酮(hfac)與上述之組合;Sn(R’’’)4
,其中R’’’是烷基、胺、醚(諸如,甲氧基(OMe)、乙氧基(OE)、異丙氧基(OiPr)、叔丁氧基(Ot-Bu))或上述之組合;及Sn(R’’’’)2
,其中R’’’’是基於環戊二烯(Cp)的配體。如圖8C所示,使用蝕刻劑去除了氟化部分並獲得了非共形蝕刻的表面345。非共形蝕刻的表面345具有V形剖面。使用蝕刻劑後殘留在表面上的氟殘留物可能是有利的中毒效果,這意味著在隨後的Al沉積過程中,可能會形成非共形膜,這有利於自下而上間隙填充。
圖9是根據一個實施例的從分子角度的蝕刻製程的示意圖。在此實施例中,NF3
電漿用作氟化物源,而TMA用作氟化鋁蝕刻劑。在此實施例中生成的混合的烷基鋁氟化合物在大約250℃之前沒有揮發性,因此在250℃以下沒有蝕刻。
在使用蝕刻劑之後,可以將膜任選地暴露於氧化劑以去除未被蝕刻劑去除的Al-F鍵。合適的氧化化學物質包括但不限於:O2
電漿(RPS和直接)、臭氧、水、N2
O以及將任何Al-F殘留物轉化回Al-O的任何其他氧化化學物質。
如果尚未完全形成間隙填充膜,則重複沉積420,隨後進行氟化430,使用蝕刻劑440以及可選的氧化470。圖8D提供了由含Al膜330部分填充的間隙的橫剖視圖。製程可以由(沉積)a→(蝕刻)b定義,其中「a」和「b」分別獨立地是沉積循環數和蝕刻循環數。在一個或多個實施例中,「a」在0至1000的範圍中而「b」在0至1000的範圍中。
間隙填充膜350在圖8E中示出,其中間隙基本上或完全地被AlCxOyNz膜填充(x、y和z獨立地在0-3的範圍內)並且沒有空隙或接縫。間隙填充膜完成後,間隙填充的基板將離開沉積/蝕刻迴路到一個或多個可選的後製程460。
後製程460之後的間隙填充膜350的橫剖面圖如圖8F所示,其中沉積在基板表面320上的含Al膜330的部分被去除,含Al膜330僅留在間隙內部。
圖10顯示了使用NF3電漿和TMA蝕刻Al2O3膜的實施例的厚度(Å)與溫度(℃)的關係圖。在200℃、250℃與290℃下用TMA/N2、NF3電漿蝕刻40Å的AlO。壓力、NF3%、循環數目與電漿功率分別為0.8T、10%、30與50W。根據圖10,在200℃時生長了一種被認為是AlF的膜。在250℃時無生長或蝕刻,在290℃時有蝕刻。這些結果表明,蝕刻速度取決於溫度。
氟化程度取決於NF3電漿處理的積極性。通過控制NF3%、電漿功率、NF3電漿脈衝長度、基板溫度和腔室壓力,可以控制氟化程度。可使表面氟化的程度最小化,以實現更可控的蝕刻製程。如果未控制氟化程度,則可以使用大脈衝TMA將所有AlF物種轉換為AlFx(CH3)y物種,並且在給出非常大的TMA脈沖之前,TMA脈衝可能不會飽和。如圖11所示,在2.5%的NF3
下,增加NF3
電漿脈衝會增加蝕刻速度。圖12顯示TMA脈衝可用2.5%NF3
飽和在0.2秒TMA脈衝下。
圖13示出了作為沉積/蝕刻循環數目的函數的蝕刻厚度(Å)的圖。溫度、壓力、NF3
%、TMA脈衝與電漿功率分別為290℃、0.8 T、2.5%、0.2 s與50 W。如圖13所示,蝕刻厚度隨循環次數的增加而線性增加。
圖14A-B提供具有溝槽特徵的10:1深寬比結構的掃描電子顯微鏡(SEM)圖像作為對照實施例。使用TMA和H2
O作為前驅物,在290℃的溫度和0.8托的壓力下通過ALD沉積了厚度約為73Å的Al2
O3
膜。沉積的膜基本上是共形的,側邊/頂比為〜0.96。
圖15A-B提供具有溝槽特徵的10:1深寬比結構在執行了一百次(沉積)a→(蝕刻)b循環(其中a=1且b=1)之後的掃描電子顯微鏡(SEM)圖像。用TMA和H2
O進行沉積部,先用NF3
電漿再進行TMA進行蝕刻。製程過程中溫度為290℃,壓力為0.8T。顯然,添加蝕刻部可沿溝槽非共形生長。側邊/頂比為〜0.67,表明沉積的膜的共形比對照(圖14A-14B)的少。
因此,揭露內容的一個或多個實施例針對利用如圖5所示的批次製程腔室的處理方法。基板60放置在具有複數個區域250a-h的製程腔室中,每個區域通過氣簾150與相鄰區域隔開。基板表面的至少一部分在製程腔室的第一處理區域250a中暴露於第一製程條件。某些實施例的第一製程條件包括含鋁前驅物。
基板表面橫向移動通過氣簾150至製程腔室的第二處理區域250b。基板表面在第二處理區域250b中暴露於第二製程條件。某些實施例的第二製程條件包括與由AlCx
Oy
Nz
表示的含鋁前驅物形成膜的反應物,其中x、y和z獨立地在0-1的範圍內。
基板表面橫向移動通過氣簾150至製程腔室的第三區域250c。然後可以在第三區域250c中將基板表面暴露於第三製程條件。某些實施例的第三製程條件包括與AlCx
Oy
Nz
膜反應形成AlF3
的氟化劑。
基板表面橫向移動通過氣簾150到製程腔室的第四區域250d。然後可以在第四區域250d中將基板表面暴露於第四製程條件。某些實施例的第四製程條件包括與AlF3
反應以生成可去除的揮發性物質的蝕刻劑。
在某些實施例中,將基板暴露於另外的第一和第二製程條件下,以形成具有預定膜厚度的膜。在某些實施例中,將基板暴露於額外的第三和第四製程條件,以重複蝕刻基板表面。
選擇性地,基板表面橫向地移動穿過氣簾150到製程腔室的第五區域250e。然後可以在第五區域250e中將基板表面暴露於第五製程條件。某些實施例的第五製程條件包括與Al-F鍵反應形成Al-O鍵的氧化劑。
根據一個或多個實施例,在形成層之前和/或之後,對基板進行處理。此處理可以在相同的腔室中進行,或在一個或多個單獨的製程腔室中進行。在某些實施例中,基板從第一腔室移至單獨的第二腔室以進行進一步處理。可將基板直接從第一腔室移動至單獨的製程腔室,或者可以將基板從第一腔室移至一個或多個移送腔室,然後再移至單獨的製程腔室。因此,處理設備可包括與移送站連通的多個腔室。此類設備可以稱為「群集工具」或「群集系統」等。
一般而言,群集工具是一種模塊化系統,包括多個執行各種功能的腔室,包括基板中心的查找和定向、脫氣、退火、沉積和/或蝕刻。根據一個或多個實施例,群集工具至少包括第一腔室和中央移送腔室。中央移送腔室可容納機器人,機器人可在製程腔室和裝載閘腔室之間穿梭基板。移送腔室通常保持在真空條件下,並提供了一個中間階段,用於將基板從一個腔室穿梭到另一個腔室和/或到位於群集工具前端的裝載閘腔室。可適用於本揭露內容的兩種眾所周知的群集工具是Centura®和Endura®,兩者均可從加利福尼亞州聖克拉拉的應用材料公司獲得。然而,為了執行本文所述的製程的特定步驟,可以改變腔室的確切佈置和組合。可使用的其他製程腔室,包括但不限於:週期性層沉積(CLD)、原子層沉積(ALD)、化學氣相沉積(CVD)、物理氣相沉積(PVD)、蝕刻、預清洗、化學清洗、例如RTP的熱處理、電漿氮化、脫氣、定向、羥基化與其他基板處理。通過在群集工具上的腔室中進行製程,在沉積後續膜之前在沒有氧化的情況下可以避免使基板表面帶有大氣雜質。
根據一個或多個實施例,基板連續處於真空或「裝載閘」條件下,並且從一個腔室移到另一個腔室時不會暴露在環境空氣中。因此,移送腔室處於真空下,並在真空壓力下被「抽空」。惰性氣體可能存在於製程腔室或移送腔室中。在某些實施例中,惰性氣體用作淨化氣體以去除部分或全部反應物。根據一個或多個實施例,在沉積腔室的出口處注入淨化氣體,以防止反應物從沉積腔室移至移送腔室和/或其他製程腔室。因此,惰性氣體流在腔室的出口處形成了一個簾幕。
可在單個基板沉積腔室中處理基板,在處理另一個基板之前,先加載、處理和卸載單個基板。基板也可以在類似於傳送帶系統的連續方式中進行處理,在該系統中,將多個基板分別裝載到腔室的第一部分中,移動穿過腔室,然後從腔室的第二部分卸載。腔室和相關輸送系統的形狀可形成直線路徑或彎曲路徑。另外,製程腔室可以是轉盤,其中多個基板圍繞中心軸移動,並在整個轉盤路徑中暴露於沉積、蝕刻、退火、清洗等製程。
在處理過程中,可以加熱或冷卻基板。上述加熱或冷卻可通過任何合適的手段來實現,包括但不限於改變基板支撐件的溫度以及使加熱或冷卻的氣體流向基板表面。在某些實施例中,基板支撐件包括加熱器/冷卻器,可以控制加熱器/冷卻器以傳導方式改變基板溫度。在一個或多個實施例中,加熱或冷卻所用氣體(反應性氣體或惰性氣體任一者)以局部改變基板溫度。在某些實施例中,加熱器/冷卻器位於腔室內基板表面附近,以對流方式改變基板溫度。
在處理過程中,基板也可以固定或旋轉。旋轉的基板可以連續旋轉或不連續旋轉。舉例而言,基板可以在整個製程中旋轉,或者基板可以在暴露於不同反應性氣體或淨化氣體之間少量旋轉。在處理過程中旋轉(連續或逐步)基板可通過最小化例如氣流幾何形狀的局部可變性的影響來幫助產生更均勻的沉積或蝕刻。
在原子層沉積型腔室中,基板可在空間或時間上分離的過程中暴露於第一和第二前驅物。時間ALD是一種傳統的製程,其中第一前驅物流入腔室以與表面反應。在流動第二前驅物之前,從腔室中清除第一前驅物。在空間ALD中,第一和第二前驅物兩者同時流向腔室,但在空間上分開,從而在前驅物流之間存在防止前驅物混合的區域。在空間ALD中,基板相對於氣體分配板移動,或氣體分配板相對於基板移動。
在方法的一個或多個部分在一個腔室中發生的實施例中,製程可以是空間ALD製程。儘管上述一種或多種化學物質可能不兼容(即導致在基板表面上以外的其他反應和/或在腔室上沉積),空間分隔確保了試劑不會在氣相中暴露於彼此。舉例而言,時間ALD涉及清除沉積腔室。然而,實際上,有時在流入另外的試劑之前不可能從腔室中清除所有過量的試劑。因此,腔室內的任何殘留試劑都可能發生反應。通過空間分離,不需要清除多餘的試劑,並且限制了交叉污染。此外,清除腔室需要花費大量時間,因此可以通過消除清除步驟來增加產量。
在整個說明書中,對「一個實施例」、「某些實施例」、「一個或多個實施例」或「實施例」的引用是指結合該實施例描述的特定特徵、結構、材料或特性被包括在揭露內容的至少一個實施例中。因此,在整個說明書中各個地方出現諸如「在一個或多個實施例中」、「在某些實施例中」、「在一個實施例中」或「在實施例中」的短語不一定是本揭露內容的相同實施例。此外,在一個或多個實施例中,特定特徵、結構、材料或特性可以任何合適的方式組合。
儘管本文中的揭露內容已經參照特定實施例進行了描述,但是應當理解,這些實施例僅是本揭露內容的原理和應用的說明。對於本領域技術人員將顯而易見的是,在不脫離本揭露內容的精神和範圍的情況下,可以對本揭露內容的方法和設備進行各種修改和變化。因此,意圖是本揭露內容包括在隨附申請專利範圍及其等同物的範圍內的修改和變化。
17:旋轉
60:基板
61:頂表面
84:區域
100:製程腔室
120:氣體分配組件
121:前表面
122:注射器單元
123:內周邊緣
124:外邊緣
125:第一反應性氣體通口
127:路徑
135:第二氣體通口
140:基座組件
141:頂表面
142:凹部
143:底面
144:邊緣
145:真空通口
150:氣簾
155:淨化氣體通口
160:支撐柱
162:致動器
170:間隙
180:裝載閘腔室
250:處理區域
250a:第一處理區域
250b:第二處理區域
250c:第三區域
250d:第四區域
250e:第五區域
250h:第八處理區域
280:工廠接口
310:特徵
312:底面
314:第一側壁
316:第二側壁
320:基板表面
330:含Al膜
340:氟化部分
345:非共形蝕刻的表面
350:間隙填充膜
400:製程
410、420、422、430、440、450、460、470:步驟
為了可以詳細地理解本揭露內容的上述特徵的方式,可以通過參考實施例來對簡要概述於上的本發明進行更詳細的描述,其中一些在附圖中示出。但是,應注意,附圖僅示出了本揭露內容的典型實施例,因此不應視為對其範圍的限制,因為揭露內容可允許其他等效的實施例。
圖1示出了根據揭露內容的一個或多個實施例的批次製程腔室的橫剖面圖;
圖2示出了根據揭露內容的一個或多個實施例的批次製程腔室的部分透視圖;
圖3示出了根據揭露內容的一個或多個實施例的批次製程腔室的示意圖;
圖4示出了用於根據揭露內容的一個或多個實施例的批次製程腔室中的楔形氣體分配組件的一部分的示意圖;
圖5示出了根據揭露內容的一個或多個實施例的批次製程腔室的示意圖;
圖6示出了根據揭露內容的一個或多個實施例的基板特徵的橫剖面圖;
圖7示出了根據揭露內容的一個或多個實施例的自下而上間隙-填充製程的製程流程圖;
圖8A至8F示出了根據揭露內容的一個或多個實施例的間隙-填充製程;
圖9是根據一個實施例的從分子角度的蝕刻製程的示意圖;
圖10示出了根據揭露內容的一個或多個實施例的厚度(Å)與溫度(℃)的關係圖;
圖11示出了根據揭露內容的一個或多個實施例的每個週期的增長和Å單位下的蝕刻作為NF3
脈衝函數的圖;
圖12示出了根據揭露內容的一個或多個實施例的蝕刻速度(Å/週期)作為TMA脈衝函數的圖;
圖13示出了根據揭露內容的一個或多個實施例的厚度(Å)作為週期數目函數的圖;
圖14A-B提供10:1深寬比結構的掃描電子顯微鏡(SEM)圖像,具有溝槽特徵作為控制實施例;及
圖15A-B提供在根據揭露內容的一個或多個實施例執行多個循環之後具有溝槽特徵的10:1深寬比結構的掃描電子顯微鏡(SEM)圖像。
國內寄存資訊 (請依寄存機構、日期、號碼順序註記)
無
國外寄存資訊 (請依寄存國家、機構、日期、號碼順序註記)
無
312:底面
314:第一側壁
316:第二側壁
320:基板表面
350:間隙填充膜
Claims (20)
- 一種處理方法,包括:在一基板表面的一特徵中以自下而上方式沉積一含鋁間隙-填充膜,該特徵具有一底面、一頂部表面與數個自該頂部表面延伸一深度至該底面的側壁,該特徵具有一由一第一側壁與一第二側壁界定的寬度,其中以自下而上方式沉積該含鋁間隙-填充膜的步驟包括在該基板表面與該特徵的該第一側壁、第二側壁與頂面上共形地沉積一含鋁膜;及藉由下述方式非共形地蝕刻沉積於該基板表面上的該含鋁膜:在該特徵的該頂部表面附近集中更多個氟化分子,以在比該底面更高的一蝕刻速率下蝕刻該特徵的該頂部附近。
- 如請求項1所述之處理方法,其中非共形地蝕刻沉積於該基板表面上的該含鋁間隙-填充膜的步驟包括依序暴露該含鋁間隙-填充膜至一含鋁前驅物、一反應物、一氟化劑和一蝕刻劑;或依序暴露該含鋁間隙-填充膜至一反應物、一含鋁前驅物、一氟化劑和一蝕刻劑。
- 如請求項2所述之處理方法,進一步包括重複藉由沉積該含鋁前驅物形成該含鋁膜以及非共形地蝕刻沉積於該基板表面上的該含鋁間隙-填充膜直到形成該含鋁間隙-填充膜,以致填充該特徵的該深度與 該寬度且沒有空隙。
- 如請求項2所述之處理方法,其中該含鋁間隙-填充膜的一厚度在一約10Å至約10000Å的範圍中。
- 如請求項2所述之處理方法,其中該含鋁間隙-填充膜包括根據AlCxOyNz的一物種,其中x、y和z獨立地在一0-3的範圍中。
- 如請求項5所述之處理方法,其中y為0。
- 如請求項2所述之處理方法,其中該含鋁前驅物包括一含烷基鋁化合物、一基於烷氧化鋁的化合物、一基於鋁氨基的化合物、一鋁鹵化物或上述之組合。
- 如請求項7所述之處理方法,其中該氟化劑包括WF6、NF3電漿、NbF5、XeF2、F2、TiF4、氟化氫(HF)、吡啶-HF、烷基胺-HF、一金屬鹵化物或上述之組合。
- 如請求項8所述之處理方法,其中該蝕刻劑包括下列一者或多者:R’3Al,其中R’是一烷基、一胺或上述之組合;Sn(R”)2,其中R”是乙醯丙酮(acac)、六氟乙醯丙酮或上述之組合;Sn(R''')4,其中R'''是一烷基、一胺、一醚或上 述之組合;及Sn(R'''')2,其中R''''是一基於環戊二烯(Cp)的配體。
- 如請求項2所述之處理方法,其中該含鋁前驅物包括三甲基鋁(TMA),該氟化劑包括NF3電漿,而該蝕刻劑包括三甲基鋁(TMA)。
- 如請求項1所述之處理方法,其中該特徵的一深寬比大於或等於5:1,其中該深寬比包括該特徵的一深度比上該特徵的一寬度的一比例。
- 如請求項1所述之處理方法,其中該含鋁間隙-填充膜沒有空隙或接縫。
- 一種處理方法,包括:將一基板表面放置在一製程腔室中,該基板表面上具有至少一個特徵,該至少一個特徵產生一具有一底部、一頂部表面和數個側壁的間隙;將該基板表面暴露於一含鋁前驅物和一反應物,以在該特徵上形成一共形含鋁膜;將該特徵上的該共形含鋁膜暴露於一氟化劑和一蝕刻劑,以藉由下述方式相對於該特徵的該底部在一較高的蝕刻速率下優先蝕刻該特徵的該頂部處的該共形含鋁膜:在該特徵的該頂部表面附近集中更多個氟化分子,以在比該底面更高的一蝕刻速率下蝕刻該特徵 的該頂部表面附近;在該優先蝕刻步驟後,可選擇性地將該特徵上的該共形含鋁膜暴露於一氧化劑;及重複依序暴露於該含鋁前驅物和該反應物然後暴露於該氟化劑和該蝕刻劑以及可選擇性的氧化劑,以自下而上方式填充該特徵的該間隙。
- 如請求項13所述之處理方法,其中該氟化劑包括一電漿。
- 如請求項14所述之處理方法,其中該電漿是一指向性電漿。
- 如請求項13所述之處理方法,其中在將該基板表面依序暴露於該含鋁前驅物和該反應物的步驟發生1次至約10000次後,蝕刻該共形含鋁膜。
- 如請求項13所述之處理方法,其中在每次將該基板表面依序暴露於該含鋁前驅物和該反應物之前,將該基板表面依序暴露於該氟化劑和該蝕刻劑,且該方法包括藉由下述方式非共形地蝕刻該基板表面上的該共形含鋁膜:在該特徵的該頂部附近集中更多個氟化分子,以在比該底部更高的一蝕刻速率下蝕刻該特徵的該頂部。
- 一種處理方法,包括:將一具有一基板表面的基板放入包含複數個部分的 製程腔室中,每個部分藉由一氣簾與相鄰部分隔開,該基板表面具有至少一個特徵,該至少一個特徵具有一頂部、底部與數個側邊以及一大於或等於10:1的深寬比,其中該深寬比包括該特徵的一深度比上該特徵的一寬度的一比例;在該製程腔室的一第一部分中將該基板表面的至少一部分暴露於一第一製程條件,該第一製程條件包括一含鋁前驅物;將該基板表面橫向移動通過一氣簾至該製程腔室的一第二部分;在該製程腔室的該第二部分中將該基板表面暴露於一第二製程條件,該第二製程條件包括一與該含鋁前驅物在該特徵上形成一共形含鋁膜的反應物,該含鋁膜包括根據AlCxOyNz的一物種,其中x、y和z獨立地在一0-3的範圍中;將具有該特徵上的該含鋁膜的該基板表面橫向移動通過一氣簾至該製程腔室的一第三部分;在該製程腔室的該第三部分中將具有該特徵上的該含鋁膜的該基板表面暴露於一第三製程條件,該第三製程條件包括一氟化劑;將具有該特徵上的該含鋁膜的該基板表面橫向移動通過一氣簾至該製程腔室的一第四部分; 在該製程腔室的該第四部分中將具有該特徵上的該含鋁膜的該基板表面暴露於一第四製程條件,該第四製程條件包括一蝕刻劑,以藉由下述方式相對於該特徵的該底部在一較高的蝕刻速率下優先蝕刻該特徵的該頂部處:在該特徵的該頂部附近集中更多個氟化分子,以在比該底部更高的一蝕刻速率下蝕刻該特徵的該頂部;及可選擇性地將具有該特徵上的該膜的該基板表面橫向移動通過一氣簾至該製程腔室的一第五部分;可選擇性地在該製程腔室的該第五部分中將具有該特徵上的該含鋁膜的該基板表面暴露於一第五製程條件,該第五製程條件包括一氧化劑;及重複暴露於該第一部分、該第二部分、該第三部分、該第四部分以及可選擇性的該第五部分,包括該基板表面的橫向移動,以用該含鋁膜共形地填充該特徵。
- 如請求項18所述之方法,其中該含鋁前驅物包括三甲基鋁(TMA),該氟化劑包括NF3電漿,而該蝕刻劑包括三甲基鋁(TMA)。
- 如請求項18所述之方法,其中該膜包括AlO或AlN,且該方法包括藉由下述方式非共形地蝕刻該基板表面上的該膜:在該特徵的該頂部附近集中更多個氟化分子,以在比該底部更高的一蝕刻速率下 蝕刻該特徵的該頂部。
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