US20150194320A1 - Metallic mask patterning process for minimizing collateral etch of an underlayer - Google Patents
Metallic mask patterning process for minimizing collateral etch of an underlayer Download PDFInfo
- Publication number
- US20150194320A1 US20150194320A1 US14/149,898 US201414149898A US2015194320A1 US 20150194320 A1 US20150194320 A1 US 20150194320A1 US 201414149898 A US201414149898 A US 201414149898A US 2015194320 A1 US2015194320 A1 US 2015194320A1
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- US
- United States
- Prior art keywords
- layer
- organic planarization
- metallic
- planarization layer
- hard mask
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims description 51
- 238000000059 patterning Methods 0.000 title description 9
- 239000003989 dielectric material Substances 0.000 claims abstract description 76
- 239000007769 metal material Substances 0.000 claims abstract description 62
- 229920002120 photoresistant polymer Polymers 0.000 claims abstract description 48
- 239000000758 substrate Substances 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims description 77
- 229910052751 metal Inorganic materials 0.000 claims description 20
- 239000002184 metal Substances 0.000 claims description 18
- 229910052710 silicon Inorganic materials 0.000 claims description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 9
- 229910045601 alloy Inorganic materials 0.000 claims description 9
- 239000000956 alloy Substances 0.000 claims description 9
- 229910044991 metal oxide Inorganic materials 0.000 claims description 9
- 150000004706 metal oxides Chemical class 0.000 claims description 9
- 239000010703 silicon Substances 0.000 claims description 9
- 238000005229 chemical vapour deposition Methods 0.000 claims description 8
- 238000004528 spin coating Methods 0.000 claims description 6
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 229920000620 organic polymer Polymers 0.000 claims description 5
- 239000002861 polymer material Substances 0.000 claims description 5
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 5
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 238000004380 ashing Methods 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000006117 anti-reflective coating Substances 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 283
- 239000004065 semiconductor Substances 0.000 description 17
- 238000012545 processing Methods 0.000 description 15
- 150000004767 nitrides Chemical class 0.000 description 9
- 238000005530 etching Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 6
- 238000000231 atomic layer deposition Methods 0.000 description 6
- 230000005669 field effect Effects 0.000 description 5
- 238000005240 physical vapour deposition Methods 0.000 description 5
- -1 HfOxNy Inorganic materials 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 238000004549 pulsed laser deposition Methods 0.000 description 4
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 3
- 239000011229 interlayer Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- 229910002244 LaAlO3 Inorganic materials 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 229910000577 Silicon-germanium Inorganic materials 0.000 description 2
- 229910002370 SrTiO3 Inorganic materials 0.000 description 2
- 229910010303 TiOxNy Inorganic materials 0.000 description 2
- 229910003134 ZrOx Inorganic materials 0.000 description 2
- LEVVHYCKPQWKOP-UHFFFAOYSA-N [Si].[Ge] Chemical compound [Si].[Ge] LEVVHYCKPQWKOP-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000005234 chemical deposition Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 229910052593 corundum Inorganic materials 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910021480 group 4 element Inorganic materials 0.000 description 2
- 239000001995 intermetallic alloy Substances 0.000 description 2
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum oxide Inorganic materials [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000001459 lithography Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- KTUFCUMIWABKDW-UHFFFAOYSA-N oxo(oxolanthaniooxy)lanthanum Chemical compound O=[La]O[La]=O KTUFCUMIWABKDW-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000005368 silicate glass Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910001845 yogo sapphire Inorganic materials 0.000 description 2
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 2
- INZDTEICWPZYJM-UHFFFAOYSA-N 1-(chloromethyl)-4-[4-(chloromethyl)phenyl]benzene Chemical compound C1=CC(CCl)=CC=C1C1=CC=C(CCl)C=C1 INZDTEICWPZYJM-UHFFFAOYSA-N 0.000 description 1
- QIJNJJZPYXGIQM-UHFFFAOYSA-N 1lambda4,2lambda4-dimolybdacyclopropa-1,2,3-triene Chemical compound [Mo]=C=[Mo] QIJNJJZPYXGIQM-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229910001339 C alloy Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910039444 MoC Inorganic materials 0.000 description 1
- 229910026551 ZrC Inorganic materials 0.000 description 1
- AXQKVSDUCKWEKE-UHFFFAOYSA-N [C].[Ge].[Si] Chemical compound [C].[Ge].[Si] AXQKVSDUCKWEKE-UHFFFAOYSA-N 0.000 description 1
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 description 1
- OQNXPQOQCWVVHP-UHFFFAOYSA-N [Si].O=[Ge] Chemical compound [Si].O=[Ge] OQNXPQOQCWVVHP-UHFFFAOYSA-N 0.000 description 1
- 229910052768 actinide Inorganic materials 0.000 description 1
- 150000001255 actinides Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- CFJRGWXELQQLSA-UHFFFAOYSA-N azanylidyneniobium Chemical compound [Nb]#N CFJRGWXELQQLSA-UHFFFAOYSA-N 0.000 description 1
- SKKMWRVAJNPLFY-UHFFFAOYSA-N azanylidynevanadium Chemical compound [V]#N SKKMWRVAJNPLFY-UHFFFAOYSA-N 0.000 description 1
- AJXBBNUQVRZRCZ-UHFFFAOYSA-N azanylidyneyttrium Chemical compound [Y]#N AJXBBNUQVRZRCZ-UHFFFAOYSA-N 0.000 description 1
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005670 electromagnetic radiation Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000000609 electron-beam lithography Methods 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
- JEGUKCSWCFPDGT-UHFFFAOYSA-N h2o hydrate Chemical compound O.O JEGUKCSWCFPDGT-UHFFFAOYSA-N 0.000 description 1
- WHJFNYXPKGDKBB-UHFFFAOYSA-N hafnium;methane Chemical compound C.[Hf] WHJFNYXPKGDKBB-UHFFFAOYSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- UNASZPQZIFZUSI-UHFFFAOYSA-N methylidyneniobium Chemical compound [Nb]#C UNASZPQZIFZUSI-UHFFFAOYSA-N 0.000 description 1
- NFFIWVVINABMKP-UHFFFAOYSA-N methylidynetantalum Chemical compound [Ta]#C NFFIWVVINABMKP-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 229910021483 silicon-carbon alloy Inorganic materials 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910003468 tantalcarbide Inorganic materials 0.000 description 1
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 description 1
- 229910003470 tongbaite Inorganic materials 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- 238000000233 ultraviolet lithography Methods 0.000 description 1
- 238000001039 wet etching Methods 0.000 description 1
- ZVWKZXLXHLZXLS-UHFFFAOYSA-N zirconium nitride Chemical compound [Zr]#N ZVWKZXLXHLZXLS-UHFFFAOYSA-N 0.000 description 1
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3105—After-treatment
- H01L21/31051—Planarisation of the insulating layers
- H01L21/31053—Planarisation of the insulating layers involving a dielectric removal step
- H01L21/31055—Planarisation of the insulating layers involving a dielectric removal step the removal being a chemical etching step, e.g. dry etching
- H01L21/31056—Planarisation of the insulating layers involving a dielectric removal step the removal being a chemical etching step, e.g. dry etching the removal being a selective chemical etching step, e.g. selective dry etching through a mask
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- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02041—Cleaning
- H01L21/02057—Cleaning during device manufacture
- H01L21/02068—Cleaning during device manufacture during, before or after processing of conductive layers, e.g. polysilicon or amorphous silicon layers
- H01L21/02071—Cleaning during device manufacture during, before or after processing of conductive layers, e.g. polysilicon or amorphous silicon layers the processing being a delineation, e.g. RIE, of conductive layers
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- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
- H01L21/02123—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon
- H01L21/02126—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC
- H01L21/0214—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC the material being a silicon oxynitride, e.g. SiON or SiON:H
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- H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
- H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
- H01L21/02263—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase
- H01L21/02271—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
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- H01L21/0271—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers
- H01L21/0273—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers characterised by the treatment of photoresist layers
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- H01L21/0276—Photolithographic processes using an anti-reflective coating
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- H01L21/033—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising inorganic layers
- H01L21/0332—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising inorganic layers characterised by their composition, e.g. multilayer masks, materials
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- H01L21/033—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising inorganic layers
- H01L21/0334—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising inorganic layers characterised by their size, orientation, disposition, behaviour, shape, in horizontal or vertical plane
- H01L21/0337—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising inorganic layers characterised by their size, orientation, disposition, behaviour, shape, in horizontal or vertical plane characterised by the process involved to create the mask, e.g. lift-off masks, sidewalls, or to modify the mask, e.g. pre-treatment, post-treatment
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- 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
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- H01L21/28008—Making conductor-insulator-semiconductor electrodes
- H01L21/28017—Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon
- H01L21/28026—Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon characterised by the conductor
- H01L21/28123—Lithography-related aspects, e.g. sub-lithography lengths; Isolation-related aspects, e.g. to solve problems arising at the crossing with the side of the device isolation; Planarisation aspects
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- 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
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- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
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- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
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- 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
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- H01L29/40—Electrodes ; Multistep manufacturing processes therefor
- H01L29/43—Electrodes ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
- H01L29/49—Metal-insulator-semiconductor electrodes, e.g. gates of MOSFET
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- H01L29/40—Electrodes ; Multistep manufacturing processes therefor
- H01L29/43—Electrodes ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
- H01L29/49—Metal-insulator-semiconductor electrodes, e.g. gates of MOSFET
- H01L29/51—Insulating materials associated therewith
- H01L29/518—Insulating materials associated therewith the insulating material containing nitrogen, e.g. nitride, oxynitride, nitrogen-doped material
Definitions
- the present disclosure relates to methods of patterning a metallic material layer on a dielectric material layer and structures for effecting the same.
- Patterning of a metallic material layer overlying a dielectric layer can result in collateral damages of the underlying dielectric layer.
- the functionality of the dielectric layer is affected by collateral damages as in the case of a gate dielectric layer, minimizing the collateral damages during the processing steps is critical in providing high performance and/or reliability in the device employing the dielectric layer.
- a patterning process for a stack of a high dielectric constant (high-k) gate dielectric layer including a dielectric metal oxide and a metallic material layer can employ an etch mask stack including a second metallic material layer in addition to a photoresist layer. While the second metallic material layer can be advantageously employed to generate a high fidelity replica of the pattern in the photoresist layer, removal of the second metallic material layer can result in collateral etch of the high-k gate dielectric layer and metallic contamination in a processing tool. Further, removal of additional materials in the etch mask stack can result in further collateral etching of the metallic material layer.
- a method is desired for patterning a metallic material layer while minimizing collateral etches of an underlying dielectric layer and avoiding metallic contamination.
- a stack of a dielectric material layer and a metallic material layer are formed on a substrate.
- a first organic planarization layer, a non-metallic hard mask layer, and a photoresist layer are sequentially deposited over the metallic material layer.
- the photoresist layer is lithographically patterned, and the pattern in the photoresist layer is transferred through the non-metallic hard mask layer, the first organic planarization layer, and the metallic material layer to form a cavity.
- a second organic planarization layer is deposited within the cavity and over remaining portions of the photoresist layer.
- the second organic planarization layer and the photoresist layer are recessed, and the non-metallic hard mask layer is subsequently removed. Remaining portions of the first and second organic planarization layers are simultaneously removed to provide physically exposed surfaces of the patterned metallic material layer and a top surface of the dielectric material layer.
- a method of forming a patterned structure is provided.
- a vertical stack is formed over a dielectric material layer on a substrate.
- the vertical stack includes, from bottom to top, a metallic material layer, a first organic planarization layer, and a non-metallic hard mask layer.
- a cavity is formed though the non-metallic hard mask layer, the first organic planarization layer, and the metallic material layer.
- a top surface of the dielectric material layer is physically exposed underneath the cavity.
- a second organic planarization layer is applied in the cavity and over the non-metallic hard mask layer. An upper portion of the second organic planarization layer is recessed.
- the non-metallic hard mask layer is removed.
- a lower portion of the second organic planarization layer and the first organic planarization layer are removed.
- the top surface of the dielectric material layer is physically exposed again.
- FIG. 1 is a vertical cross-sectional view of an exemplary structure after formation of a stack including a dielectric material layer, a metallic material layer, a first organic planarization layer, a dielectric mask layer, and a patterned photoresist layer on a substrate according to an embodiment of the present disclosure.
- FIG. 2 is a vertical cross-sectional view of the exemplary structure after transfer of the pattern of in the photoresist layer into the dielectric mask layer, the first organic planarization layer, and the first metallic material layer by a set of at least one etch according to an embodiment of the present disclosure.
- FIG. 3 is a vertical cross-sectional view of the exemplary structure after application of a second organic planarization layer according to an embodiment of the present disclosure.
- FIG. 4 is a vertical cross-sectional view of the exemplary structure after recessing the second organic planarization layer and collateral removal of any remaining portion of the photoresist layer according to an embodiment of the present disclosure.
- FIG. 5 is a vertical cross-sectional view of the exemplary structure after removal of the dielectric mask layer according to an embodiment of the present disclosure.
- FIG. 6 is a vertical cross-sectional view of the exemplary structure after removal of the first and second organic planarization layers according to an embodiment of the present disclosure.
- FIG. 7 is a vertical cross-sectional view of a variation of the exemplary structure after application of a second organic planarization layer according to an embodiment of the present disclosure.
- the present disclosure relates to methods of patterning a metallic material layer on a dielectric material layer and structures for effecting the same, which are now described in detail with accompanying figures. It is noted that like and corresponding elements are referred to by like reference numerals.
- the drawings are not in scale.
- ordinals such as “first” and “second” are employed merely to distinguish similar elements, and different ordinals may be employed to designate a same element in the specification and/or claims.
- an exemplary structure includes a material stack formed on a substrate 10 .
- the material stack includes, from bottom to top, of a dielectric material layer 20 , a metallic material layer 30 , a first organic planarization layer 40 , a dielectric mask layer 50 , and a patterned photoresist layer 57 .
- the substrate 10 can include any solid material.
- the substrate 10 can include at least one semiconductor material, at least one conductive material, at least one dielectric material, or a combination or a stack thereof.
- Semiconductor materials that can be included in the substrate 10 include, but are not limited to, an elemental semiconductor material such as silicon or germanium; an alloy of Group IV elements such as a silicon-germanium alloy, a silicon-carbon alloy, and a silicon-germanium-carbon alloy; a compound semiconductor material; an organic semiconductor material; and combinations thereof.
- Metallic material that can be included in the substrate 10 include, but are not limited to, an elemental metal, an intermetallic alloy, a conductive metallic nitride, a conductive metallic carbide, and combinations and alloys thereof.
- Dielectric materials that can be included in the substrate 10 include, but are not limited to, a dielectric oxide of at least one semiconductor element such as silicon oxide, a dielectric nitride of at least one semiconductor element such as silicon nitride, a dielectric metal oxide, a dielectric metal nitride, and combinations and alloys thereof.
- the substrate 10 can be sufficiently thick to provide mechanical support for the material stack thereupon.
- the thickness of the substrate 10 can be in a range from 30 microns to 1 mm, although lesser and greater thicknesses can also be employed.
- the topmost portion of the substrate 10 can include a semiconductor layer embedding various doped semiconductor material portions.
- the substrate 10 can include source and drain regions of field effect transistors that are formed in a semiconductor material portion.
- the semiconductor material portion can be a planar semiconductor portion laterally surrounded by a shallow trench isolation structure (not shown) and having a top surface that is coplanar with the topmost surface of the substrate 10 , or can be a semiconductor fin as known in the art.
- the topmost portion of the substrate 10 can include a metal interconnect structure including at least one interlayer dielectric (ILD) material layer and at least one metal line structure and/or at least one metal via structure as known in the art.
- the topmost portions of the substrate can include a dielectric material such as silicon oxide, silicon nitride, porous or non-porous organosilicate glass, or combinations thereof.
- at least one metal line structure and/or at least one metal via structure can include a metallic material such as copper, aluminum, tungsten, a metallic nitride, a metallic carbide, or a combination thereof.
- the dielectric material layer 20 can include any dielectric material.
- the dielectric material layer 20 can include a dielectric material that is known to be suitable for a gate dielectric of a field effect transistor.
- the thickness of the dielectric material layer 20 can be in a range from 1 nm to 20 nm, although lesser and greater thicknesses can also be employed.
- the dielectric material layer 20 can include a dielectric oxide of at least one semiconductor element such as silicon oxide or a silicon-germanium oxide, or a dielectric oxynitride of at least one semiconductor element such as silicon oxynitride or a silicon-germanium oxynitride.
- the dielectric material layer 20 can include a high dielectric constant (high-k) dielectric material.
- a high-k dielectric material refers to a dielectric material having a dielectric constant greater than 7.9.
- the high-k dielectric material of the dielectric material layer 20 can include a dielectric metal oxide.
- Exemplary high-k dielectric materials that can be employed for dielectric material layer 20 include, but are not limited to, HfO 2 , ZrO 2 , La 2 O 3 , Al 2 O 3 , TiO 2 , SrTiO 3 , LaAlO 3 , Y 2 O 3 , HfO x N y , ZrO x N y , La 2 O x N y , Al 2 O x N y , TiO x N y , SrTiO x N y , LaAlO x N y , Y 2 O x N y , a silicate thereof, and an alloy thereof.
- the high-k dielectric material can be selected from HfO 2 , ZrO 2 , and TiO 2 .
- the first high-k dielectric material can be HfO 2 .
- the first high-k dielectric material can be deposited by methods well known in the art including, for example, chemical vapor deposition (CVD), physical vapor deposition (PVD), molecular beam deposition (MBD), pulsed laser deposition (PLD), liquid source misted chemical deposition (LSMCD), atomic layer deposition (ALD), etc.
- the dielectric material layer 20 can include a dielectric material that is known to be suitable for an interlayer dielectric (ILD) material.
- the dielectric material layer 20 can include porous or non-porous organosilicate glass (OSG), doped silicate glass, undoped silicate glass, silicon nitride, silicon oxynitride, nitrogen-doped organosilicate glass, or combinations thereof.
- the dielectric constant of the material of the dielectric material layer 20 can be in a range from 2.0 to 3.9.
- the interlayer dielectric material can be deposited, for example, by chemical vapor deposition, spin-coating, or a combination thereof.
- the thickness of the dielectric material layer 20 can be in a range from 10 nm to 300 nm, although lesser and greater thicknesses can also be employed.
- the metallic material layer 30 can include an elemental metal, an alloy of at least two elemental metals, a compound of at least one metal and nitrogen, a compound of at least one metal and carbon, or a stack thereof.
- the metallic material layer 30 can include any elemental metal, which can be an elemental transition metal, a Lanthanide, an Actinide, an alkali metal, or an alkaline earth metal.
- the metallic material layer 30 can include an intermetallic alloy of at least two elemental metals.
- the metallic material layer includes a metallic nitride, a metallic carbide, or an alloy or a stack thereof.
- Exemplary metallic nitride materials that can be employed for the metallic material layer 30 include, but are not limited to, titanium nitride, tantalum nitride, tungsten nitride, aluminum nitride, yttrium nitride, zirconium nitride, vanadium nitride, niobium nitride, and other nitrides of at least one metallic element.
- Exemplary metallic carbide materials that can be employed for the metallic material layer 30 include, but are not limited to, titanium carbide, tantalum carbide, tungsten carbide, zirconium carbide, vanadium carbide, niobium carbide, hafnium carbide, chromium carbide, molybdenum carbide, and other carbides of at least one metallic element.
- the metallic material layer 30 can include a stack of multiple metallic layers having different compositions.
- the metallic material layer 30 can be deposited, for example, by physical vapor deposition (sputtering), chemical vapor deposition, atomic layer deposition, or a combination thereof.
- the thickness of the metallic material layer 30 can be in a range from 1 nm to 30 nm, although lesser and greater thicknesses can also be employed.
- the first organic planarization layer 40 includes an organic planarization material as known in the art.
- the organic planarization material of the first organic planarization layer 40 is herein referred to as a first organic planarization material.
- the first organic planarization layer 40 can include a non-photosensitive organic polymer material.
- a “non-photosensitive” material refers to a material that does not change chemical property upon irradiation for lithographic exposure employing a conventional light wavelength and a conventional dose level for exposure as known in the art.
- Exemplary materials that can be employed for the first organic planarization layer 40 include ODL-102, commercially available from ShinEtsu Chemical Co. Ltd.; HM8006 and HM8014, commercially available from JSR Corporation; and CHM701B, commercially available from Cheil Chemical Co. Ltd.
- the first organic planarization layer 40 can be formed, for example, by a spin-on coating.
- the thickness of the first organic planarization layer 40 can be in a range from 30 nm to 600 nm, although lesser and greater thicknesses can also be employed.
- the non-metallic hard mask layer 50 includes a non-metallic non-photosensitive material.
- the non-metallic hard mask layer 50 can include a dielectric oxide, a dielectric nitride, or a dielectric oxynitride including a group IV element.
- the non-metallic hard mask layer 50 can include a silicon oxide material, a silicon nitride material, or a silicon oxynitride material.
- the non-metallic hard mask layer 50 can be deposited by chemical vapor deposition, atomic layer deposition, spin coating, or a combination thereof.
- the non-metallic hard mask layer 50 can include a nitrogen-containing organosilicate glass (OSG), which includes Si, C, O, H, and N.
- OSG nitrogen-containing organosilicate glass
- An exemplary material for a nitrogen-containing OSG is NBLoKTM available from Applied Materials, Inc.
- the non-metallic hard mask layer 50 can include a silicon-containing antireflective coating (Si-ARC) material as known in the art.
- the Si-ARC material can be a polymer containing Si with organic units or halide bound to the silicon, which are generally polysiloxanes.
- the Si-ARC material can include more than 30% in atomic concentration of silicon.
- the Si-ARC material can be applied, for example, by spin coating, and can be cured at an elevated temperature around 220° C. during a post application bake (PAB) process.
- PAB post application bake
- the non-metallic hard mask layer 50 can include a dielectric metal oxide.
- dielectric metal oxides include, but are not limited to, HfO 2 , ZrO 2 , La 2 O 3 , Al 2 O 3 , TiO 2 , SrTiO 3 , LaAlO 3 , Y 2 O 3 , HfO x N y , ZrO x N y , La 2 O x N y , Al 2 O x N y , TiO x N y , SrTiO x N y , LaAlO x N y , Y 2 O x N y , a silicate thereof, and an alloy thereof.
- Each value of x is independently from 0.5 to 3 and each value of y is independently from 0 to 2.
- the dielectric metal oxide material can be deposited by methods well known in the art including, for example, chemical vapor deposition (CVD), physical vapor deposition (PVD), molecular beam deposition (MBD), pulsed laser deposition (PLD), liquid source misted chemical deposition (LSMCD), atomic layer deposition (ALD), etc.
- CVD chemical vapor deposition
- PVD physical vapor deposition
- MBD molecular beam deposition
- PLD pulsed laser deposition
- LSMCD liquid source misted chemical deposition
- ALD atomic layer deposition
- the thickness of the non-metallic hard mask layer 50 can be in a range from 1 nm to 30 nm, although lesser and greater thicknesses can also be employed. In one embodiment, the thickness of the non-metallic hard mask layer 50 can be in a range from 3 nm to 10 nm.
- the patterned photoresist layer 57 includes a photoresist material.
- the patterned photoresist layer 57 can be formed by forming a blanket photoresist material layer over the top surface of the non-metallic hard mask layer 50 by spin coating, lithographically exposing the blanket photoresist material layer by electromagnetic radiation or by an electron beam, and developing the lithographically exposed photoresist material layer.
- the thickness of the blanket photoresist material layer can be in a range from 50 nm to 1,000 nm, although lesser and greater thicknesses can also be employed.
- the lithographic exposure of the blanket photoresist layer can be performed by deep ultraviolet (DUV) lithography, mid-ultraviolet lithography (MUV), grayscale lithography, electron beam lithography, or a combination thereof.
- DUV deep ultraviolet
- UUV mid-ultraviolet lithography
- the development process can remove lithographically exposed portions selective to lithographically unexposed portions of the photoresist material, or can remove lithographically unexposed portions of the photoresist material selective to the lithographically exposed portions of the photoresist material.
- the patterned photoresist layer 57 includes at least one opening therein. A portion of the top surface of the non-metallic hard mask layer 50 is physically exposed underneath each opening in the patterned photoresist layer 57 .
- the pattern of the opening in the patterned photoresist layer 57 corresponds to the area from which removal of the metallic material layer 30 is desired.
- the area of the remaining portions of the patterned photoresist layer 57 corresponds to the area in which preservation of the metallic material layer 30 is desired after patterning of the metallic material layer 30 .
- the pattern in the patterned photoresist layer 57 is transferred through the stack of the non-metallic hard mask layer 50 , the first organic planarization layer 40 , and the metallic material layer 30 by at least one etch.
- at least one anisotropic etch can be employed among the at least one etch that transfers the pattern in the patterned photoresist layer 57 is transferred through the stack of the non-metallic hard mask layer 50 , the first organic planarization layer 40 , and the metallic material layer 30 .
- a cavity 59 is formed though the non-metallic hard mask layer 50 , the first organic planarization layer 40 , and the metallic material layer 30 .
- a top surface of the dielectric material layer 20 is physically exposed underneath the cavity 59 .
- the non-metallic hard mask layer 50 can be etched, for example, by an anisotropic etch or an isotropic etch.
- the etch chemistry for etching the non-metallic hard mask layer 50 can be selected based on the material of the non-metallic hard mask layer as known in the art.
- the patterned photoresist layer 57 is employed as an etch mask during the etching of unmasked portions of the non-metallic hard mask layer 50 .
- the non-metallic hard mask layer 50 can be etched by a reactive ion etch, which is an anisotropic etch.
- the non-metallic hard mask layer 50 can be etched by a wet etch, which is an isotropic etch.
- the portion(s) of the first organic planarization layer 40 underlying each opening in the patterned photoresist layer 57 can be etched by another etch.
- the first organic planarization layer 40 can be etched employing an anisotropic etch process, which forms vertical sidewalls in the first organic planarization layer 40 as the etch process proceeds.
- the patterned photoresist layer 57 can be vertically recessed during the etching of the first organic planarization layer 40 .
- a cavity 59 is formed in the first organic planarization layer 40 underneath each opening in the patterned photoresist layer 57 .
- the patterned photoresist layer 57 can be completely consumed before, or at the time of, the cavity 59 reaching the interface between the first organic planarization layer 40 and the metallic material layer.
- the sidewalls of the non-metallic hard mask layer 50 and the sidewalls of the first organic planarization layer 40 can be vertically coincident among one another after formation of the cavity 59 .
- a first surface and a second surface are vertically coincident with each other if the first surface overlies, or underlies, the second surface and a vertical plane including the first surface and the second surface exists.
- the physically exposed portion of the metallic material layer 30 underlying the cavity 59 can be subsequently removed by another etch, which can be an isotropic etch or an anisotropic etch.
- the physical exposed portion of the metallic material layer 30 can be removed by a wet etch.
- the chemistry of the etch process employed to etch the metallic material layer 30 can be selected to avoid damaging the material of the dielectric material layer 20 . Suitable etch chemistries known in the art can be employed to etch the metallic material layer 30 while minimizing collateral etching of the dielectric material layer 20 . Methods for selective wet etching of metal nitrides can be found, for example, in United States Patent Application No. 2006/0226122A1.
- the metallic material layer 30 can be etched selective to the dielectric oxide material by a wet etch employing a mixture of hydrogen peroxide and ethylenediaminetetraacetic acid.
- a 1:1 mixture of hydrogen peroxide and ethylenediaminetetraacetic acid elevated to a temperature of 60° C. or higher can be employed to etch a titanium nitride film selective to a dielectric metal oxide material.
- a second organic planarization layer 60 is deposited in the cavity 59 (See FIG. 2 ) and over the non-metallic hard mask layer 50 .
- the second organic planarization layer 60 is deposited into the cavity 59 and over the non-metallic hard mask layer 50 .
- the second organic planarization layer 60 can be formed directly on a top surface and sidewalls of the remaining portion of the non-metallic hard mask layer 50 that remains after the at least one anisotropic etch that forms the cavity 59 and the etch process that forms an opening in the metallic material layer 30 .
- the second organic planarization layer 60 can include any organic planarization material that can be employed as the first organic planarization layer 40 .
- the organic planarization material of the second organic planarization layer 60 is herein referred to as a second organic planarization material.
- the first organic planarization material and the second organic planarization material may, or may not, be the same as the organic planarization material of the first organic planarization material layer 40 .
- each of the first and second organic planarization layers ( 40 , 60 ) can include a non-photosensitive organic polymer material.
- the non-photosensitive organic polymer material of the second organic planarization layer 60 can be selected independent of the non-photosensitive organic polymer material of the first organic planarization layer 40 .
- the second organic planarization layer 60 can be applied, for example, by spin coating of an organic planarization material.
- a dimple may be present on the top surface of the second organic planarization layer 60 over the volume of each cavity 59 (See FIG. 2 ) that is filled with the organic planarization material of the second organic planarization layer 60 .
- the thickness of the second organic planarization layer 60 as measured above the top surface of the non-metallic hard mask layer 50 , may be in a range from 1 nm to 300 nm, although lesser and greater thicknesses can also be employed.
- the topmost surface of the second organic planarization layer 60 may be formed below the horizontal plane including the top surface of the non-metallic hard mask layer 50 .
- the second organic planarization layer 60 can be employed to minimize additional collateral etching of the dielectric material layer 20 after the patterning of the metallic material layer 30 and during the removal of the non-metallic hard mask layer 59 , and the first organic planarization layer 40 .
- the organic planarization material of the second organic planarization layer 60 that is present on the top surface of the dielectric material layer 20 protects the dielectric material layer 20 during subsequent processing steps for removal of the non-metallic hard mask layer 59 , and during an initial portion of the processing step for removal of the first organic planarization layer 40 .
- an upper portion of the second organic planarization layer 60 is recessed by an etch process or by an ashing process such that the recessed top surface of the second organic planarization layer 60 is present below the horizontal plane including the top surface of the non-metallic hard mask layer 50 .
- the upper portion of the second organic planarization layer 60 can be removed by a dry etch.
- the dry etch can be an anisotropic etch such as a reactive ion etch, or an isotropic etch as chemical downstream etch.
- the upper portion of the second organic planarization layer 60 can be removed by an ashing process, in which the organic planarization material of the second organic planarization layer 60 combines with oxygen, becomes volatilized, and is removed in a gas phase out of a processing chamber.
- the recessing of the upper portion of the second organic planarization layer 60 can be performed employing an etch process that is selective to the material of the non-metallic hard mask layer 50 . In another embodiment, the recessing of the upper portion of the second organic planarization layer 60 can be performed employing an etch process that is not selective to the material of the non-metallic hard mask layer 50 .
- the second planarization layer 60 partially fills each cavity within the vertical stack of the metallic material layer 30 , the first organic planarization layer 40 , and the non-metallic hard mask layer 50 (if present).
- the top surface of the remaining portion of the second organic planarization layer 60 within each cavity may have a concave top surface due to a dimple in the top surface of the second organic planarization layer 60 as formed at the processing step of FIG. 3 and due to the geometrical effects of the cavity 59 during the recessing of the second organic planarization layer 60 .
- the dielectric mask layer 50 if not collaterally etched during the recessing of the second organic planarization layer 60 at the processing step of FIG. 4 , can be removed.
- the removal of the dielectric mask layer 50 can be performed by an etch, which can be an anisotropic etch such as a reactive ion etch or an isotropic etch such as a wet etch.
- the etch process that is employed to remove the dielectric mask layer 50 may, or may not, be selective to the materials of the first organic planarization layer 40 and/or the second organic planarization layer 60 .
- a suitable etch chemistry may be employed to remove the non-metallic hard mask layer 50 as known in the art.
- the presence of the organic planarization material of the second organic planarization layer 60 on the top surface of the dielectric material layer 20 provides protection for the top surface of the dielectric material layer 20 underlying the cavity 59 from collateral etching during the removal of the non-metallic hard mask layer 50 .
- the remaining lower portion of the second organic planarization layer 60 and the first organic planarization layer 40 are removed selective to the dielectric material in the dielectric material layer 20 .
- the lower portion of the second organic planarization layer 60 and the first organic planarization layer 40 are removed simultaneously employing a same etch process.
- the lower portion of the second organic planarization layer 60 and the first organic planarization layer 40 can be removed by an ashing process, in which the organic planarization materials of the first and second organic planarization layers ( 40 , 60 ) combine with oxygen, become volatilized, and are removed in a gas phase out of a processing chamber.
- the lower portion of the second organic planarization layer 60 and the first organic planarization layer 40 can be removed by a dry etch.
- the dry etch can be an anisotropic etch such as a reactive ion etch, or an isotropic etch as chemical downstream etch.
- the simultaneous removal of the lower portion of the second organic planarization layer 60 and the first organic planarization layer 40 can be performed employing a process that is selective to the material of the dielectric material layer 20 .
- the height of the recessed top surface of the second organic planarization layer 60 during the recess etch at the processing step of FIG. 4 can be selected such that the top surface of the dielectric material layer 20 and the top surface of the metallic material layer 30 become physically exposed simultaneously, or with minimal differences in time.
- the overetch time needed to remove bottommost portions of the first and second organic planarization layers ( 40 , 60 ) can be minimized, thereby minimizing any collateral damage to the physically exposed top surface of the dielectric material layer 20 .
- a surface clean process may be performed to remove any residual material derived from the first and second organic planarization layers ( 40 , 60 ).
- a wet clean employing the SC1 etch chemistry can be performed to remove organic residues from the top surfaces of the dielectric material layer 20 and the metallic material layer 30 .
- the SC1 etch chemistry can employ, for example, a 1:1:5 solution of 27 volume % of ammonium hydroxide in water, 30 volume % of hydrogen peroxide in water, and deionized water at a temperature range about 80° C. The duration of the wet etch can be optimized based on the thickness of the metallic material layer 30 .
- Additional material stacks can be subsequently deposited on the exemplary structure illustrated in FIG. 6 .
- Such additional material stacks can include another metallic material layer and/or a doped or undoped semiconductor material layer and/or another dielectric material layer as known in the art.
- a vertical cross-sectional view of a variation of the exemplary structure is shown at the processing step corresponding to the processing step of FIG. 3 for the exemplary structure.
- the patterned photoresist layer 57 may not be completely consumed during the processing steps of FIG. 2 .
- the second organic planarization layer 60 is deposited into the cavity 59 and directly on a top surface and sidewalls of the patterned photoresist layer 57 , the sidewalls of the non-metallic hard mask layer 50 , the sidewalls of the first organic planarization layer 40 , the sidewalls of the metallic material layer 30 , and the top surface of the dielectric material layer 20 .
- FIGS. 4-6 can be performed to provide the exemplary structure illustrated in FIG. 6 .
- the remaining portions of the patterned photoresist layer 57 can be removed collaterally during the processing step of FIG. 4 , i.e., during the recessing of the second organic planarization layer 60 .
- the various methods of the present disclosure can be employed to provide a dielectric material layer 20 in contact with a bottom surface of a patterned metallic material layer 30 while minimizing structural or chemical damages to the physically exposed portions of the dielectric material layer 20 .
- the methods of the present disclosure can be advantageously employed in any device structure that requires a dielectric material layer with structural and chemical integrity, i.e., a dielectric material layer with no, or minimal, structural and chemical changes in the dielectric material in regions that do not contact the metallic material layer 30 .
- An exemplary application of the methods of the present disclosure is patterning of a work function material layer formed directly on a top surface of a high-k dielectric material layer during formation of gate electrodes for field effect transistors.
- the high-k dielectric material layer can be the dielectric material layer 20 of the present disclosure
- the work function material layer can be the metallic material layer 30 of the present disclosure.
- the high-k dielectric material layer can be a predominant portion of gate dielectrics for the field effect transistors. As such, any structural or chemical damage to the high-k dielectric material layer can be detrimental to performance and/or reliability of the field effect transistors that employ the high-k dielectric material layer as gate dielectrics.
- the methods of the present disclosure enhances the performance and/or the reliability of semiconductor devices employing the dielectric material layer 20 .
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Abstract
Description
- The present disclosure relates to methods of patterning a metallic material layer on a dielectric material layer and structures for effecting the same.
- Patterning of a metallic material layer overlying a dielectric layer can result in collateral damages of the underlying dielectric layer. In case the functionality of the dielectric layer is affected by collateral damages as in the case of a gate dielectric layer, minimizing the collateral damages during the processing steps is critical in providing high performance and/or reliability in the device employing the dielectric layer.
- For example, a patterning process for a stack of a high dielectric constant (high-k) gate dielectric layer including a dielectric metal oxide and a metallic material layer can employ an etch mask stack including a second metallic material layer in addition to a photoresist layer. While the second metallic material layer can be advantageously employed to generate a high fidelity replica of the pattern in the photoresist layer, removal of the second metallic material layer can result in collateral etch of the high-k gate dielectric layer and metallic contamination in a processing tool. Further, removal of additional materials in the etch mask stack can result in further collateral etching of the metallic material layer. Thus, a method is desired for patterning a metallic material layer while minimizing collateral etches of an underlying dielectric layer and avoiding metallic contamination.
- A stack of a dielectric material layer and a metallic material layer are formed on a substrate. A first organic planarization layer, a non-metallic hard mask layer, and a photoresist layer are sequentially deposited over the metallic material layer. The photoresist layer is lithographically patterned, and the pattern in the photoresist layer is transferred through the non-metallic hard mask layer, the first organic planarization layer, and the metallic material layer to form a cavity. A second organic planarization layer is deposited within the cavity and over remaining portions of the photoresist layer. The second organic planarization layer and the photoresist layer are recessed, and the non-metallic hard mask layer is subsequently removed. Remaining portions of the first and second organic planarization layers are simultaneously removed to provide physically exposed surfaces of the patterned metallic material layer and a top surface of the dielectric material layer.
- According to an aspect of the present disclosure, a method of forming a patterned structure is provided. A vertical stack is formed over a dielectric material layer on a substrate. The vertical stack includes, from bottom to top, a metallic material layer, a first organic planarization layer, and a non-metallic hard mask layer. A cavity is formed though the non-metallic hard mask layer, the first organic planarization layer, and the metallic material layer. A top surface of the dielectric material layer is physically exposed underneath the cavity. A second organic planarization layer is applied in the cavity and over the non-metallic hard mask layer. An upper portion of the second organic planarization layer is recessed. The non-metallic hard mask layer is removed. A lower portion of the second organic planarization layer and the first organic planarization layer are removed. The top surface of the dielectric material layer is physically exposed again.
-
FIG. 1 is a vertical cross-sectional view of an exemplary structure after formation of a stack including a dielectric material layer, a metallic material layer, a first organic planarization layer, a dielectric mask layer, and a patterned photoresist layer on a substrate according to an embodiment of the present disclosure. -
FIG. 2 is a vertical cross-sectional view of the exemplary structure after transfer of the pattern of in the photoresist layer into the dielectric mask layer, the first organic planarization layer, and the first metallic material layer by a set of at least one etch according to an embodiment of the present disclosure. -
FIG. 3 is a vertical cross-sectional view of the exemplary structure after application of a second organic planarization layer according to an embodiment of the present disclosure. -
FIG. 4 is a vertical cross-sectional view of the exemplary structure after recessing the second organic planarization layer and collateral removal of any remaining portion of the photoresist layer according to an embodiment of the present disclosure. -
FIG. 5 is a vertical cross-sectional view of the exemplary structure after removal of the dielectric mask layer according to an embodiment of the present disclosure. -
FIG. 6 is a vertical cross-sectional view of the exemplary structure after removal of the first and second organic planarization layers according to an embodiment of the present disclosure. -
FIG. 7 is a vertical cross-sectional view of a variation of the exemplary structure after application of a second organic planarization layer according to an embodiment of the present disclosure. - As stated above, the present disclosure relates to methods of patterning a metallic material layer on a dielectric material layer and structures for effecting the same, which are now described in detail with accompanying figures. It is noted that like and corresponding elements are referred to by like reference numerals. The drawings are not in scale. As used herein, ordinals such as “first” and “second” are employed merely to distinguish similar elements, and different ordinals may be employed to designate a same element in the specification and/or claims.
- Referring to
FIG. 1 , an exemplary structure according to an embodiment of the present disclosure includes a material stack formed on asubstrate 10. The material stack includes, from bottom to top, of adielectric material layer 20, ametallic material layer 30, a firstorganic planarization layer 40, adielectric mask layer 50, and a patternedphotoresist layer 57. - The
substrate 10 can include any solid material. Thesubstrate 10 can include at least one semiconductor material, at least one conductive material, at least one dielectric material, or a combination or a stack thereof. Semiconductor materials that can be included in thesubstrate 10 include, but are not limited to, an elemental semiconductor material such as silicon or germanium; an alloy of Group IV elements such as a silicon-germanium alloy, a silicon-carbon alloy, and a silicon-germanium-carbon alloy; a compound semiconductor material; an organic semiconductor material; and combinations thereof. Metallic material that can be included in thesubstrate 10 include, but are not limited to, an elemental metal, an intermetallic alloy, a conductive metallic nitride, a conductive metallic carbide, and combinations and alloys thereof. Dielectric materials that can be included in thesubstrate 10 include, but are not limited to, a dielectric oxide of at least one semiconductor element such as silicon oxide, a dielectric nitride of at least one semiconductor element such as silicon nitride, a dielectric metal oxide, a dielectric metal nitride, and combinations and alloys thereof. - In one embodiment, the
substrate 10 can be sufficiently thick to provide mechanical support for the material stack thereupon. In one embodiment, the thickness of thesubstrate 10 can be in a range from 30 microns to 1 mm, although lesser and greater thicknesses can also be employed. - In one embodiment, the topmost portion of the
substrate 10 can include a semiconductor layer embedding various doped semiconductor material portions. For example, thesubstrate 10 can include source and drain regions of field effect transistors that are formed in a semiconductor material portion. The semiconductor material portion can be a planar semiconductor portion laterally surrounded by a shallow trench isolation structure (not shown) and having a top surface that is coplanar with the topmost surface of thesubstrate 10, or can be a semiconductor fin as known in the art. - In one embodiment, the topmost portion of the
substrate 10 can include a metal interconnect structure including at least one interlayer dielectric (ILD) material layer and at least one metal line structure and/or at least one metal via structure as known in the art. In this case, the topmost portions of the substrate can include a dielectric material such as silicon oxide, silicon nitride, porous or non-porous organosilicate glass, or combinations thereof. Further, at least one metal line structure and/or at least one metal via structure, if present, can include a metallic material such as copper, aluminum, tungsten, a metallic nitride, a metallic carbide, or a combination thereof. - The
dielectric material layer 20 can include any dielectric material. In one embodiment, thedielectric material layer 20 can include a dielectric material that is known to be suitable for a gate dielectric of a field effect transistor. The thickness of thedielectric material layer 20 can be in a range from 1 nm to 20 nm, although lesser and greater thicknesses can also be employed. In one embodiment, thedielectric material layer 20 can include a dielectric oxide of at least one semiconductor element such as silicon oxide or a silicon-germanium oxide, or a dielectric oxynitride of at least one semiconductor element such as silicon oxynitride or a silicon-germanium oxynitride. - In another embodiment, the
dielectric material layer 20 can include a high dielectric constant (high-k) dielectric material. As used herein, a high-k dielectric material refers to a dielectric material having a dielectric constant greater than 7.9. In one embodiment, the high-k dielectric material of thedielectric material layer 20 can include a dielectric metal oxide. Exemplary high-k dielectric materials that can be employed fordielectric material layer 20 include, but are not limited to, HfO2, ZrO2, La2O3, Al2O3, TiO2, SrTiO3, LaAlO3, Y2O3, HfOxNy, ZrOxNy, La2OxNy, Al2OxNy, TiOxNy, SrTiOxNy, LaAlOxNy, Y2OxNy, a silicate thereof, and an alloy thereof. Each value of x is independently from 0.5 to 3 and each value of y is independently from 0 to 2. In one embodiment, the high-k dielectric material can be selected from HfO2, ZrO2, and TiO2. In one embodiment, the first high-k dielectric material can be HfO2. The first high-k dielectric material can be deposited by methods well known in the art including, for example, chemical vapor deposition (CVD), physical vapor deposition (PVD), molecular beam deposition (MBD), pulsed laser deposition (PLD), liquid source misted chemical deposition (LSMCD), atomic layer deposition (ALD), etc. - In one embodiment, the
dielectric material layer 20 can include a dielectric material that is known to be suitable for an interlayer dielectric (ILD) material. For example, thedielectric material layer 20 can include porous or non-porous organosilicate glass (OSG), doped silicate glass, undoped silicate glass, silicon nitride, silicon oxynitride, nitrogen-doped organosilicate glass, or combinations thereof. In this case, the dielectric constant of the material of thedielectric material layer 20 can be in a range from 2.0 to 3.9. The interlayer dielectric material can be deposited, for example, by chemical vapor deposition, spin-coating, or a combination thereof. The thickness of thedielectric material layer 20 can be in a range from 10 nm to 300 nm, although lesser and greater thicknesses can also be employed. - The
metallic material layer 30 can include an elemental metal, an alloy of at least two elemental metals, a compound of at least one metal and nitrogen, a compound of at least one metal and carbon, or a stack thereof. In one embodiment, themetallic material layer 30 can include any elemental metal, which can be an elemental transition metal, a Lanthanide, an Actinide, an alkali metal, or an alkaline earth metal. In another embodiment, themetallic material layer 30 can include an intermetallic alloy of at least two elemental metals. In one embodiment, the metallic material layer includes a metallic nitride, a metallic carbide, or an alloy or a stack thereof. Exemplary metallic nitride materials that can be employed for themetallic material layer 30 include, but are not limited to, titanium nitride, tantalum nitride, tungsten nitride, aluminum nitride, yttrium nitride, zirconium nitride, vanadium nitride, niobium nitride, and other nitrides of at least one metallic element. Exemplary metallic carbide materials that can be employed for themetallic material layer 30 include, but are not limited to, titanium carbide, tantalum carbide, tungsten carbide, zirconium carbide, vanadium carbide, niobium carbide, hafnium carbide, chromium carbide, molybdenum carbide, and other carbides of at least one metallic element. In one embodiment, themetallic material layer 30 can include a stack of multiple metallic layers having different compositions. - The
metallic material layer 30 can be deposited, for example, by physical vapor deposition (sputtering), chemical vapor deposition, atomic layer deposition, or a combination thereof. The thickness of themetallic material layer 30 can be in a range from 1 nm to 30 nm, although lesser and greater thicknesses can also be employed. - The first
organic planarization layer 40 includes an organic planarization material as known in the art. The organic planarization material of the firstorganic planarization layer 40 is herein referred to as a first organic planarization material. In one embodiment, the firstorganic planarization layer 40 can include a non-photosensitive organic polymer material. As used herein, a “non-photosensitive” material refers to a material that does not change chemical property upon irradiation for lithographic exposure employing a conventional light wavelength and a conventional dose level for exposure as known in the art. Exemplary materials that can be employed for the firstorganic planarization layer 40 include ODL-102, commercially available from ShinEtsu Chemical Co. Ltd.; HM8006 and HM8014, commercially available from JSR Corporation; and CHM701B, commercially available from Cheil Chemical Co. Ltd. - The first
organic planarization layer 40 can be formed, for example, by a spin-on coating. The thickness of the firstorganic planarization layer 40 can be in a range from 30 nm to 600 nm, although lesser and greater thicknesses can also be employed. - The non-metallic
hard mask layer 50 includes a non-metallic non-photosensitive material. In one embodiment, the non-metallichard mask layer 50 can include a dielectric oxide, a dielectric nitride, or a dielectric oxynitride including a group IV element. For example, the non-metallichard mask layer 50 can include a silicon oxide material, a silicon nitride material, or a silicon oxynitride material. In this case, the non-metallichard mask layer 50 can be deposited by chemical vapor deposition, atomic layer deposition, spin coating, or a combination thereof. - In another embodiment, the non-metallic
hard mask layer 50 can include a nitrogen-containing organosilicate glass (OSG), which includes Si, C, O, H, and N. An exemplary material for a nitrogen-containing OSG is NBLoK™ available from Applied Materials, Inc. - In yet another embodiment, the non-metallic
hard mask layer 50 can include a silicon-containing antireflective coating (Si-ARC) material as known in the art. The Si-ARC material can be a polymer containing Si with organic units or halide bound to the silicon, which are generally polysiloxanes. The Si-ARC material can include more than 30% in atomic concentration of silicon. The Si-ARC material can be applied, for example, by spin coating, and can be cured at an elevated temperature around 220° C. during a post application bake (PAB) process. - In still another embodiment, the non-metallic
hard mask layer 50 can include a dielectric metal oxide. Exemplary dielectric metal oxides include, but are not limited to, HfO2, ZrO2, La2O3, Al2O3, TiO2, SrTiO3, LaAlO3, Y2O3, HfOxNy, ZrOxNy, La2OxNy, Al2OxNy, TiOxNy, SrTiOxNy, LaAlOxNy, Y2OxNy, a silicate thereof, and an alloy thereof. Each value of x is independently from 0.5 to 3 and each value of y is independently from 0 to 2. The dielectric metal oxide material can be deposited by methods well known in the art including, for example, chemical vapor deposition (CVD), physical vapor deposition (PVD), molecular beam deposition (MBD), pulsed laser deposition (PLD), liquid source misted chemical deposition (LSMCD), atomic layer deposition (ALD), etc. - The thickness of the non-metallic
hard mask layer 50 can be in a range from 1 nm to 30 nm, although lesser and greater thicknesses can also be employed. In one embodiment, the thickness of the non-metallichard mask layer 50 can be in a range from 3 nm to 10 nm. - The patterned
photoresist layer 57 includes a photoresist material. The patternedphotoresist layer 57 can be formed by forming a blanket photoresist material layer over the top surface of the non-metallichard mask layer 50 by spin coating, lithographically exposing the blanket photoresist material layer by electromagnetic radiation or by an electron beam, and developing the lithographically exposed photoresist material layer. The thickness of the blanket photoresist material layer can be in a range from 50 nm to 1,000 nm, although lesser and greater thicknesses can also be employed. The lithographic exposure of the blanket photoresist layer can be performed by deep ultraviolet (DUV) lithography, mid-ultraviolet lithography (MUV), grayscale lithography, electron beam lithography, or a combination thereof. Depending on the nature of the photoresist material, the development process can remove lithographically exposed portions selective to lithographically unexposed portions of the photoresist material, or can remove lithographically unexposed portions of the photoresist material selective to the lithographically exposed portions of the photoresist material. - The patterned
photoresist layer 57 includes at least one opening therein. A portion of the top surface of the non-metallichard mask layer 50 is physically exposed underneath each opening in the patternedphotoresist layer 57. The pattern of the opening in the patternedphotoresist layer 57 corresponds to the area from which removal of themetallic material layer 30 is desired. The area of the remaining portions of the patternedphotoresist layer 57 corresponds to the area in which preservation of themetallic material layer 30 is desired after patterning of themetallic material layer 30. - Referring to
FIG. 2 , the pattern in the patternedphotoresist layer 57 is transferred through the stack of the non-metallichard mask layer 50, the firstorganic planarization layer 40, and themetallic material layer 30 by at least one etch. In one embodiment, at least one anisotropic etch can be employed among the at least one etch that transfers the pattern in the patternedphotoresist layer 57 is transferred through the stack of the non-metallichard mask layer 50, the firstorganic planarization layer 40, and themetallic material layer 30. Acavity 59 is formed though the non-metallichard mask layer 50, the firstorganic planarization layer 40, and themetallic material layer 30. A top surface of thedielectric material layer 20 is physically exposed underneath thecavity 59. - The non-metallic
hard mask layer 50 can be etched, for example, by an anisotropic etch or an isotropic etch. The etch chemistry for etching the non-metallichard mask layer 50 can be selected based on the material of the non-metallic hard mask layer as known in the art. The patternedphotoresist layer 57 is employed as an etch mask during the etching of unmasked portions of the non-metallichard mask layer 50. In one embodiment, the non-metallichard mask layer 50 can be etched by a reactive ion etch, which is an anisotropic etch. In another embodiment, the non-metallichard mask layer 50 can be etched by a wet etch, which is an isotropic etch. - Subsequently, the portion(s) of the first
organic planarization layer 40 underlying each opening in the patternedphotoresist layer 57 can be etched by another etch. In one embodiment, the firstorganic planarization layer 40 can be etched employing an anisotropic etch process, which forms vertical sidewalls in the firstorganic planarization layer 40 as the etch process proceeds. The patternedphotoresist layer 57 can be vertically recessed during the etching of the firstorganic planarization layer 40. Acavity 59 is formed in the firstorganic planarization layer 40 underneath each opening in the patternedphotoresist layer 57. In one embodiment, the patternedphotoresist layer 57 can be completely consumed before, or at the time of, thecavity 59 reaching the interface between the firstorganic planarization layer 40 and the metallic material layer. In one embodiment, the sidewalls of the non-metallichard mask layer 50 and the sidewalls of the firstorganic planarization layer 40 can be vertically coincident among one another after formation of thecavity 59. As used herein, a first surface and a second surface are vertically coincident with each other if the first surface overlies, or underlies, the second surface and a vertical plane including the first surface and the second surface exists. - The physically exposed portion of the
metallic material layer 30 underlying thecavity 59 can be subsequently removed by another etch, which can be an isotropic etch or an anisotropic etch. In one embodiment, the physical exposed portion of themetallic material layer 30 can be removed by a wet etch. In one embodiment, the chemistry of the etch process employed to etch themetallic material layer 30 can be selected to avoid damaging the material of thedielectric material layer 20. Suitable etch chemistries known in the art can be employed to etch themetallic material layer 30 while minimizing collateral etching of thedielectric material layer 20. Methods for selective wet etching of metal nitrides can be found, for example, in United States Patent Application No. 2006/0226122A1. In another example, if themetallic material layer 30 includes titanium nitride and if thedielectric material layer 20 includes a dielectric metal oxide, themetallic material layer 30 can be etched selective to the dielectric oxide material by a wet etch employing a mixture of hydrogen peroxide and ethylenediaminetetraacetic acid. In an illustrative example, a 1:1 mixture of hydrogen peroxide and ethylenediaminetetraacetic acid elevated to a temperature of 60° C. or higher can be employed to etch a titanium nitride film selective to a dielectric metal oxide material. - Referring to
FIG. 3 , a secondorganic planarization layer 60 is deposited in the cavity 59 (SeeFIG. 2 ) and over the non-metallichard mask layer 50. Specifically, the secondorganic planarization layer 60 is deposited into thecavity 59 and over the non-metallichard mask layer 50. The secondorganic planarization layer 60 can be formed directly on a top surface and sidewalls of the remaining portion of the non-metallichard mask layer 50 that remains after the at least one anisotropic etch that forms thecavity 59 and the etch process that forms an opening in themetallic material layer 30. - The second
organic planarization layer 60 can include any organic planarization material that can be employed as the firstorganic planarization layer 40. The organic planarization material of the secondorganic planarization layer 60 is herein referred to as a second organic planarization material. The first organic planarization material and the second organic planarization material may, or may not, be the same as the organic planarization material of the first organicplanarization material layer 40. In one embodiment, each of the first and second organic planarization layers (40, 60) can include a non-photosensitive organic polymer material. In this case, the non-photosensitive organic polymer material of the secondorganic planarization layer 60 can be selected independent of the non-photosensitive organic polymer material of the firstorganic planarization layer 40. - The second
organic planarization layer 60 can be applied, for example, by spin coating of an organic planarization material. In one embodiment, a dimple may be present on the top surface of the secondorganic planarization layer 60 over the volume of each cavity 59 (SeeFIG. 2 ) that is filled with the organic planarization material of the secondorganic planarization layer 60. The thickness of the secondorganic planarization layer 60, as measured above the top surface of the non-metallichard mask layer 50, may be in a range from 1 nm to 300 nm, although lesser and greater thicknesses can also be employed. Alternatively, the topmost surface of the secondorganic planarization layer 60 may be formed below the horizontal plane including the top surface of the non-metallichard mask layer 50. - The second
organic planarization layer 60 can be employed to minimize additional collateral etching of thedielectric material layer 20 after the patterning of themetallic material layer 30 and during the removal of the non-metallichard mask layer 59, and the firstorganic planarization layer 40. Specifically, the organic planarization material of the secondorganic planarization layer 60 that is present on the top surface of thedielectric material layer 20 protects thedielectric material layer 20 during subsequent processing steps for removal of the non-metallichard mask layer 59, and during an initial portion of the processing step for removal of the firstorganic planarization layer 40. - Referring to
FIG. 4 , an upper portion of the secondorganic planarization layer 60 is recessed by an etch process or by an ashing process such that the recessed top surface of the secondorganic planarization layer 60 is present below the horizontal plane including the top surface of the non-metallichard mask layer 50. - In one embodiment, the upper portion of the second
organic planarization layer 60 can be removed by a dry etch. The dry etch can be an anisotropic etch such as a reactive ion etch, or an isotropic etch as chemical downstream etch. In one embodiment, the upper portion of the secondorganic planarization layer 60 can be removed by an ashing process, in which the organic planarization material of the secondorganic planarization layer 60 combines with oxygen, becomes volatilized, and is removed in a gas phase out of a processing chamber. - In one embodiment, the recessing of the upper portion of the second
organic planarization layer 60 can be performed employing an etch process that is selective to the material of the non-metallichard mask layer 50. In another embodiment, the recessing of the upper portion of the secondorganic planarization layer 60 can be performed employing an etch process that is not selective to the material of the non-metallichard mask layer 50. - The
second planarization layer 60 partially fills each cavity within the vertical stack of themetallic material layer 30, the firstorganic planarization layer 40, and the non-metallic hard mask layer 50 (if present). In one embodiment, the top surface of the remaining portion of the secondorganic planarization layer 60 within each cavity may have a concave top surface due to a dimple in the top surface of the secondorganic planarization layer 60 as formed at the processing step ofFIG. 3 and due to the geometrical effects of thecavity 59 during the recessing of the secondorganic planarization layer 60. - Referring to
FIG. 5 , thedielectric mask layer 50, if not collaterally etched during the recessing of the secondorganic planarization layer 60 at the processing step ofFIG. 4 , can be removed. The removal of thedielectric mask layer 50 can be performed by an etch, which can be an anisotropic etch such as a reactive ion etch or an isotropic etch such as a wet etch. The etch process that is employed to remove thedielectric mask layer 50 may, or may not, be selective to the materials of the firstorganic planarization layer 40 and/or the secondorganic planarization layer 60. A suitable etch chemistry may be employed to remove the non-metallichard mask layer 50 as known in the art. The presence of the organic planarization material of the secondorganic planarization layer 60 on the top surface of thedielectric material layer 20 provides protection for the top surface of thedielectric material layer 20 underlying thecavity 59 from collateral etching during the removal of the non-metallichard mask layer 50. - Referring to
FIG. 6 , the remaining lower portion of the secondorganic planarization layer 60 and the firstorganic planarization layer 40 are removed selective to the dielectric material in thedielectric material layer 20. The lower portion of the secondorganic planarization layer 60 and the firstorganic planarization layer 40 are removed simultaneously employing a same etch process. - In one embodiment, the lower portion of the second
organic planarization layer 60 and the firstorganic planarization layer 40 can be removed by an ashing process, in which the organic planarization materials of the first and second organic planarization layers (40, 60) combine with oxygen, become volatilized, and are removed in a gas phase out of a processing chamber. In another embodiment, the lower portion of the secondorganic planarization layer 60 and the firstorganic planarization layer 40 can be removed by a dry etch. The dry etch can be an anisotropic etch such as a reactive ion etch, or an isotropic etch as chemical downstream etch. - The simultaneous removal of the lower portion of the second
organic planarization layer 60 and the firstorganic planarization layer 40 can be performed employing a process that is selective to the material of thedielectric material layer 20. In one embodiment, the height of the recessed top surface of the secondorganic planarization layer 60 during the recess etch at the processing step ofFIG. 4 can be selected such that the top surface of thedielectric material layer 20 and the top surface of themetallic material layer 30 become physically exposed simultaneously, or with minimal differences in time. In this case, the overetch time needed to remove bottommost portions of the first and second organic planarization layers (40, 60) can be minimized, thereby minimizing any collateral damage to the physically exposed top surface of thedielectric material layer 20. - After removal of the remaining lower portion of the second
organic planarization layer 60 and the firstorganic planarization layer 40, the top surface of thedielectric material layer 20 within the region of thecavity 59 becomes physically exposed again. Optionally, a surface clean process may be performed to remove any residual material derived from the first and second organic planarization layers (40, 60). For example, a wet clean employing the SC1 etch chemistry can be performed to remove organic residues from the top surfaces of thedielectric material layer 20 and themetallic material layer 30. The SC1 etch chemistry can employ, for example, a 1:1:5 solution of 27 volume % of ammonium hydroxide in water, 30 volume % of hydrogen peroxide in water, and deionized water at a temperature range about 80° C. The duration of the wet etch can be optimized based on the thickness of themetallic material layer 30. - Additional material stacks can be subsequently deposited on the exemplary structure illustrated in
FIG. 6 . Such additional material stacks can include another metallic material layer and/or a doped or undoped semiconductor material layer and/or another dielectric material layer as known in the art. - Referring to
FIG. 7 , a vertical cross-sectional view of a variation of the exemplary structure is shown at the processing step corresponding to the processing step ofFIG. 3 for the exemplary structure. In the variation of the exemplary structure, the patternedphotoresist layer 57 may not be completely consumed during the processing steps ofFIG. 2 . The secondorganic planarization layer 60 is deposited into thecavity 59 and directly on a top surface and sidewalls of the patternedphotoresist layer 57, the sidewalls of the non-metallichard mask layer 50, the sidewalls of the firstorganic planarization layer 40, the sidewalls of themetallic material layer 30, and the top surface of thedielectric material layer 20. - Subsequently, the processing steps of
FIGS. 4-6 can be performed to provide the exemplary structure illustrated inFIG. 6 . The remaining portions of the patternedphotoresist layer 57 can be removed collaterally during the processing step ofFIG. 4 , i.e., during the recessing of the secondorganic planarization layer 60. - The various methods of the present disclosure can be employed to provide a
dielectric material layer 20 in contact with a bottom surface of a patternedmetallic material layer 30 while minimizing structural or chemical damages to the physically exposed portions of thedielectric material layer 20. The methods of the present disclosure can be advantageously employed in any device structure that requires a dielectric material layer with structural and chemical integrity, i.e., a dielectric material layer with no, or minimal, structural and chemical changes in the dielectric material in regions that do not contact themetallic material layer 30. - An exemplary application of the methods of the present disclosure is patterning of a work function material layer formed directly on a top surface of a high-k dielectric material layer during formation of gate electrodes for field effect transistors. In this case, the high-k dielectric material layer can be the
dielectric material layer 20 of the present disclosure, and the work function material layer can be themetallic material layer 30 of the present disclosure. The high-k dielectric material layer can be a predominant portion of gate dielectrics for the field effect transistors. As such, any structural or chemical damage to the high-k dielectric material layer can be detrimental to performance and/or reliability of the field effect transistors that employ the high-k dielectric material layer as gate dielectrics. By minimizing the collateral etching during the processing steps for removal of the non-metallichard mask layer 50, the methods of the present disclosure enhances the performance and/or the reliability of semiconductor devices employing thedielectric material layer 20. - While the disclosure has been described in terms of specific embodiments, it is evident in view of the foregoing description that numerous alternatives, modifications and variations will be apparent to those skilled in the art. Each of the various embodiments of the present disclosure can be implemented alone, or in combination with any other embodiments of the present disclosure unless expressly disclosed otherwise or otherwise impossible as would be known to one of ordinary skill in the art. Accordingly, the disclosure is intended to encompass all such alternatives, modifications and variations which fall within the scope and spirit of the disclosure and the following claims.
Claims (20)
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