TW457555B - Surface passivation using silicon oxynitride - Google Patents
Surface passivation using silicon oxynitride Download PDFInfo
- Publication number
- TW457555B TW457555B TW088103302A TW88103302A TW457555B TW 457555 B TW457555 B TW 457555B TW 088103302 A TW088103302 A TW 088103302A TW 88103302 A TW88103302 A TW 88103302A TW 457555 B TW457555 B TW 457555B
- Authority
- TW
- Taiwan
- Prior art keywords
- layer
- hydrogen
- passivation
- surface state
- silicon
- Prior art date
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- 238000002161 passivation Methods 0.000 title claims abstract description 33
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title claims abstract description 19
- 229910052710 silicon Inorganic materials 0.000 title claims abstract description 19
- 239000010703 silicon Substances 0.000 title claims abstract description 19
- 239000001257 hydrogen Substances 0.000 claims abstract description 39
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 39
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 36
- 238000000034 method Methods 0.000 claims abstract description 27
- 230000008569 process Effects 0.000 claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 claims description 18
- 239000004065 semiconductor Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 2
- NCMAYWHYXSWFGB-UHFFFAOYSA-N [Si].[N+][O-] Chemical compound [Si].[N+][O-] NCMAYWHYXSWFGB-UHFFFAOYSA-N 0.000 claims 1
- 239000010410 layer Substances 0.000 description 88
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 37
- 229910052581 Si3N4 Inorganic materials 0.000 description 31
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 31
- 239000010408 film Substances 0.000 description 27
- 150000004767 nitrides Chemical class 0.000 description 26
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 25
- 235000012431 wafers Nutrition 0.000 description 24
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 18
- 238000012360 testing method Methods 0.000 description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 13
- 238000000137 annealing Methods 0.000 description 13
- 238000012545 processing Methods 0.000 description 13
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 11
- 230000004888 barrier function Effects 0.000 description 10
- 239000003990 capacitor Substances 0.000 description 9
- 229910021332 silicide Inorganic materials 0.000 description 9
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 8
- 239000002131 composite material Substances 0.000 description 7
- 238000000151 deposition Methods 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 7
- 229910052721 tungsten Inorganic materials 0.000 description 7
- 239000010937 tungsten Substances 0.000 description 7
- 230000008021 deposition Effects 0.000 description 6
- 238000009792 diffusion process Methods 0.000 description 6
- 238000005516 engineering process Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 230000002079 cooperative effect Effects 0.000 description 5
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 5
- 125000006850 spacer group Chemical group 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000005380 borophosphosilicate glass Substances 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000006870 function Effects 0.000 description 4
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 230000002093 peripheral effect Effects 0.000 description 3
- 230000006798 recombination Effects 0.000 description 3
- 238000005215 recombination Methods 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- ZKMNUMMKYBVTFN-HNNXBMFYSA-N (S)-ropivacaine Chemical compound CCCN1CCCC[C@H]1C(=O)NC1=C(C)C=CC=C1C ZKMNUMMKYBVTFN-HNNXBMFYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000003989 dielectric material Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- -1 nitrogen oxide dichlorosilane Chemical compound 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000005360 phosphosilicate glass Substances 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 230000008439 repair process Effects 0.000 description 2
- 235000015170 shellfish Nutrition 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- WQJQOUPTWCFRMM-UHFFFAOYSA-N tungsten disilicide Chemical compound [Si]#[W]#[Si] WQJQOUPTWCFRMM-UHFFFAOYSA-N 0.000 description 2
- 229910021342 tungsten silicide Inorganic materials 0.000 description 2
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910003915 SiCl2H2 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000005264 electron capture Effects 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 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
- 229910000449 hafnium oxide Inorganic materials 0.000 description 1
- WIHZLLGSGQNAGK-UHFFFAOYSA-N hafnium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Hf+4] WIHZLLGSGQNAGK-UHFFFAOYSA-N 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000003870 refractory metal Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229910021341 titanium silicide 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
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- 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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- H01L21/00—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
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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
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- 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
- H01L21/0217—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 being a silicon nitride not containing oxygen, e.g. SixNy or SixByNz
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- H01L21/02107—Forming insulating materials on a substrate
- 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
- H01L21/02205—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 the layer being characterised by the precursor material for deposition
- H01L21/02208—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 the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si
- H01L21/02211—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 the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si the compound being a silane, e.g. disilane, methylsilane or chlorosilane
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- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- 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
- H01L21/02274—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 in the presence of a plasma [PECVD]
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- 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
- H01L21/28008—Making conductor-insulator-semiconductor electrodes
- H01L21/28017—Making conductor-insulator-semiconductor electrodes the insulator being formed after the semiconductor body, the semiconductor being silicon
- H01L21/28158—Making the insulator
- H01L21/28167—Making the insulator on single crystalline silicon, e.g. using a liquid, i.e. chemical oxidation
- H01L21/28176—Making the insulator on single crystalline silicon, e.g. using a liquid, i.e. chemical oxidation with a treatment, e.g. annealing, after the formation of the definitive gate conductor
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- 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
- H01L21/3003—Hydrogenation or deuterisation, e.g. using atomic hydrogen from a plasma
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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
- H01L21/314—Inorganic layers
- H01L21/3143—Inorganic layers composed of alternated layers or of mixtures of nitrides and oxides or of oxinitrides, e.g. formation of oxinitride by oxidation of nitride layers
- H01L21/3145—Inorganic layers composed of alternated layers or of mixtures of nitrides and oxides or of oxinitrides, e.g. formation of oxinitride by oxidation of nitride layers formed by deposition from a gas or vapour
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- H10B—ELECTRONIC MEMORY DEVICES
- H10B12/00—Dynamic random access memory [DRAM] devices
- H10B12/01—Manufacture or treatment
- H10B12/02—Manufacture or treatment for one transistor one-capacitor [1T-1C] memory cells
- H10B12/05—Making the transistor
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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
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02296—Forming insulating materials on a substrate characterised by the treatment performed before or after the formation of the layer
- H01L21/02299—Forming insulating materials on a substrate characterised by the treatment performed before or after the formation of the layer pre-treatment
- H01L21/02304—Forming insulating materials on a substrate characterised by the treatment performed before or after the formation of the layer pre-treatment formation of intermediate layers, e.g. buffer layers, layers to improve adhesion, lattice match or diffusion barriers
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- H10B—ELECTRONIC MEMORY DEVICES
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- H10B12/02—Manufacture or treatment for one transistor one-capacitor [1T-1C] memory cells
- H10B12/03—Making the capacitor or connections thereto
- H10B12/038—Making the capacitor or connections thereto the capacitor being in a trench in the substrate
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- Engineering & Computer Science (AREA)
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- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
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- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Chemical & Material Sciences (AREA)
- Plasma & Fusion (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Formation Of Insulating Films (AREA)
- Internal Circuitry In Semiconductor Integrated Circuit Devices (AREA)
- Insulated Gate Type Field-Effect Transistor (AREA)
- Semiconductor Memories (AREA)
Description
总§7555 A7 B7 一- ----------—......... ..... 五、發明说明(j ) 發明之領域 本發明係有關於裝置及裝置製造,並且更特別地是有關 於具有促成表面狀態鈍化用之層的裝匱及製造該裝置的製 程。 發明之背景 在裝置製造中,絕緣性、半導體性與導電性等諸層係被 製作並刻劃於一基板上以形成諸如.電晶體、電容以及電阻 等裝置結構。這些裝置將被相互連結以獲得所欲之電功能 。各裝置層的製作及刻割係使用諸如氧化、植入、沈積' 矽的磊晶成長、微影及蝕刻等傳統製造技術而獲得。該技 術係說明於 S.M.Sze 所著的 “VLSI Technology" ,2nd ed., New York, McGiaw-Hi丨1, 19 88 »在此倂入本案以爲參考 資料。 經濟部中央標準局J工消費合作社印製 (請先閱讀背面之注意事一.:填寫本頁) 傳統製造技術將使裝置中的諸層產生缺陷及損傷•例如 ,在半導體界面之化學鍵的損傷將形成表面或界面狀態的 懸空鍵。表面狀態將促成電子電洞對的再結合。再結合係 爲電子電洞對相消的現象。特別是發生於諸如隔離周圍及 閘極氧化物等重要的裝置界面上的在結合將產生漏電流·» 漏電流將改變閘極啓始電壓、資料遲滯及裝置的待機電源 消耗。因此,界面狀態對於裝置功能有負面影W。 表面狀態係藉由提供氫原子以鈍化懸空鍵而修復。典型 地在大約400 -600 °C的含氫氣氛中之高溫退火係用以供應 氫而鈍化懸空鍵。鈍化退火通常於裝置製:造程序後段執行
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J 本紙張尺度%用中國國家標準(CNS ) Μ規格(210X297公釐)‘ ' ’':…r ν' 457555 A7 B7 五、發明説明u ) ,諸如包含金屬化或互連層等諸層形成後。此舉將減少修 復先前製程所形成之懸空鍵所需的鈍化退火數。減少鈍化 退火數將節省製程成本。 然而,目前的互連組織及裝置結構易於阻礙氫原子到達 再結合位置以鈍化懸空鍵的能力。故將減少鈍化退火的效 益及效率。例如,以低壓化學氣相沈積法(LPCVD )所沈積之 作爲移動離子及過度金屬阻障的氮.化矽將阻止氫擴散。該 LPCVD氮化矽膜將阻止氫滲入下層,而鈍化存在於該層中 的表面狀態》在鎢柱結構中,鎢將壓制氫,而產生類似於 氮化矽層的效果。鈍化退火的效益將進一步減少,因爲氮 氣通常係用以稀釋氫(形成氣體),以減少氫氣的爆炸性。 如上述,有效地鈍化爲裝匱製造技術所引起的表面狀態 係爲所需。 發明之槪要 經濟部中央標隼局員工消费合作社印裝 (诗先閏讀背面之注意事¾也寫本頁) 本發明係有關於裝置製造。如本技藝所熟知,傳統裝置 製造技術將損傷化學鍵,而於半導體界面形成表面狀態》 這些表面狀態係藉由在氫氣退火期間供應氫原子而被修復 或鈍化》然而,目前的裝置結構易於使氫無法到達及鈍化 表面狀態》 爲克服目前裝置結構所存在的鈍化問題,一用於製造裝 置的製程係被掲示》該製程包含製造促成表面狀態鈍化之 裝置結構的步驟*該裝置結構包含氮氧化物層。在一實施 例中,該氮氧化物層係以電漿輔肋化學氣孭許積法(PECVD) Ί !
• I -4- ' 本纸張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 457555 Α7 Β7 五、發明説明(3 ) 形成。 圖式之簡略說明 第1圖係說明具有隔離之簡化的傳統電晶體裝置結構: 第2圖係說明具有鈍化層之簡化的電晶體裝置結構: 第3圖係說明具有爲複合閘極之部分的鈍化.層之簡化的 電晶體裝置結構; 第4圖係表示氮氧化物之折射係數與蝕刻選擇性間的關 係: 第5A-B圖係表示以ΑΜΕ及Nove 1 lus加工系統所製作的 氮氧化物膜周邊漏電: 第6圖係爲比較具有傳統氮化物膜之裝置與具有富氫 < Η - R )氮化物膜之裝置的漏電流的圖式: 第7圖係爲比較傳統低壓化學氣相沈積氮化膜與H-R氮 化物膜特徵的圖式:以及 第8圖示鍵結於氫之矽百分比對ND周邊漏電間的關係。 發明詳細說明 經濟部中央標準局員工消費合作社印掣 (請先閲讀背面之注意事功填寫本頁) 本發明係有關於裝置製造期間所形成之表面狀態的鈍化 «爲用於作爲舉例的目的,本發明將以動態隨機存取記憶 體(DRAM )單元做說明。然而,本發明係明顯地更爲廣泛並 延伸至諸如雙載體裝置、BiCMOS、薄膜電晶體、異質接面 裝置及相似者等裝置之製造。 在第1圖中,其係表示形成於諸如半導體晶圓等基板100 的DRAM單元101。該晶圓包含諸如以Czochralski技術所 形成的矽β晶圓的主表面並不重要,而諸如,(l〇Q )(11〇)或
Λ I 本纸張尺度適用中國國家標準(CNS ) Α4規格(210X 297公釐)
4 5 7 5 5S A7 B7 五、發明説明(4* ) (m)等任何適當的取向皆可使用。該晶圓係典型地具有 (100)取向,因爲該晶圓具有低表面狀態及高載體移動而常 被使用B其他諸如鍺、砷化鎵及ΠΙ-ν族化合物等其他半 導體晶圓亦可使用《此外,包括複數材料層之晶圓亦可使 用。這些基板包含諸如形成於另一種單晶材料上的一單晶 材料(例如,矽茌藍寶石上(SOS )),或著在非晶質材料層 上再結晶的非晶質或多晶材料C例如,矽在絕緣體上(S0J) )·其係得以以諸如硼'磷、砷或銻等雜質原子大量或微 量植入,以獲得所欲的電性。 如所示,該DRAM單元包含用以儲存代表資料位元之電荷 的電容器105。在所舉例的實施例中,該電容器係爲彤成 於基板中的溝渠電容器》諸如堆疊電容器等其他形式的電 容器亦可用於儲存電荷•包含閘極110、源極120及汲極 130的電晶體106係電連接至電容器。一淺溝渠隔離區140 係被設置以將DRAM單元與陣列中的其他單元或裝置隔離
D 經濟部中夬標準局貝工消費合作社印製 (诗先閱讀背面之注^唞寫本頁) 複數個記憶胞係成橫豎排列以形成DRAM陣列。橫列係稱 爲字元線而縱欄係稱爲位元線。通常,源極120係連接至 位元線,而閘極110係連接至或代表DRAM陣列的字元線。 藉由加諸適當的電壓於位元線及字元線,該電晶體係被開 啓而連接至電容器。 電晶體的閘極區典型地包含形成於閛極氧化物Π1上的 多晶矽層1 1 2 ·在部份應用中,一矽化物層1 1 4係甩以形
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__________________ I 本紙張尺度適用中國國家標牟(CNS > A4現格(210X297公釐} 4 5 7 5 b ΐ: A 7 B7 五、發明説明U ) 成一複合閘極堆疊。包含矽化鉬(MoSix)、矽化鉅(TaSix) ,矽化鎢(WS ί X )、矽化鈦(T i S i X )或矽化鈷(CoS i X )的矽化 物皆被用以形成層11 4 β此外’鋁或諸如鎢與鉬等耐火金 屬係單獨被使用或著結合矽化物或多晶矽使用。複合閘極 係爲所欲,因使用其可減少閘極區的片電阻’而減少沿其 傳遞之訊號的R-C延遲。 一氮化物覆蓋1】6係以低壓化學.氣相沈積法(LPCVD )沈 積於閘極上。該覆蓋係作爲後序製程用的蝕刻阻絕,諸如 形成無邊際位元線接觸於源極時。一間隔160係沈積於閘 極上,以限制源極與汲極區的向上擴散進入閘極區,其將 減少重叠電容。間隔形成後,一氮化物層1 70係沈積於閛 極邊緣以及源極' 汲極與ST1區上,以提供移動離子阻障 並作爲蝕刻阻絕。一介電層(未示)係形成於裝置結構上 ,以提供導電層間的絕緣(除非接觸係爲所欲),或作爲 保護層以將裝置結構與雜質、水氣及刮傷隔絕。該介電層 包含諸如磷矽酸鹽玻璃(PSG)或硼磷矽酸鹽玻璃(BPSG)等 摻磷二氧化矽· 經濟部中央橾準局員工消費合作社印製 (請先閲讀背面之注意事-"$寫本頁) 當然,如第1圖所示的裝置結構因作爲舉例的目的而被 簡化。例如,使用於DRAM單元中的實際裝置結構包含諸如 井、接觸及局部互連等其他區域。裝置結構之各區域的形 成係爲所熟知,並說明於諸如Kenney等人所著的ABuried Plate Trench Cell For a 64M DRAM , VLSI Tech . Di g( 1992 ) ,在此倂入本案以爲參考資料。 .. 本紙張尺度適用中國國家標隼(CNS ) AMU ( 210X297公釐) 45755 經濟部中央樣準局負工消費合作社印製 Α7 Β7 五、發明説明(6) 在裝置結構諸層製造期間所形成的表面狀態係以“” 號表示。如所示,該表面狀態係位於閘極氧化物及ST1周 圍。這些表面狀態需加以鈍化。氫退火通常係用以鈍化該 表面狀態。在退火期間,氣氛中的氫原子將穿過閛極而達 結構主體。然而,目前大部份的裝置結構皆以LPCVD氮化 矽層覆蓋。如上述,該氮化物層將阻礙氫原子穿透其以鈍 化表面狀態。 爲克服由使用傳統LPCVD氮化物層所引起的問題,一鈍 化層係被設置以完成在製造期間所產生之表面狀態的修復 。該鈍化結構包含混入裝置的一富氫(H-R)氮化矽層。如本 技藝所熟知1傅統的LPCVD氮化矽層包含大約3-5«的氫原 子(本掲示中所有的組成百分比皆以原子%表示)> 詳閱 Habraken 等人所著的 Silicon Nitride and Oxynitride Films, Mat. Sci. and Eng., R12 No.3(July 1994),以 及 C h o w 等人所著的 H y d r o g e n C ο n t e n t o f a V a r i e t y o f Plasma-DepositedSiliconNitrides, J. Appl. Phys., Vol 53, No. 8(August 1 982 ),在此倂入本案以爲參考資料。 在此所使用的"富氫"意指氫比例大於傳統LPCVD氮化矽 層。實驗顯示使用H-R氮化矽層可減少接面漏電流,亦即 成功的表面狀態鈍化。 H-R氮化矽層如何促成表面狀態鈍化的機構並不得而知 a然而,其確信H-R氮化物層係作爲氫原子源或允許氫穿 過的結構或二考的結合》所增加的氫百分比將增加H-R氮 本紙張尺度適用中國國家標準(CNS ) A4C格(2I0X 297公釐) (請先閲讀背面之注意事項 哄寫本頁) 、ye 4 5 7:: 經濟部中央標準局貝工消費合作社印製 A7 B7 五、發明説明(7 ) 化矽層中的氫原子量,而形成氫原子振散源以鈍化表面狀 態。此外’由於氫百分比增加,故氮化物層密度將減少。 密度減少將使氫原子明顯地滲透氮化物層,並進入表面狀 態鈍化用的裝置結構· 第2圖係表示諸如具有H-R矽層之DRAM單元中所使用的 —簡化裝置結構200。如所示^該11-1?氮化矽層係混入裝 置結構,以做爲裝置互連界面的阻.障或襯墊層260。裝置 結構200包含一閘極210、一汲極220、~源極230及STI 區240。閘極210包含一多晶矽層212,一諸如WSix的矽 化物層及一氮化矽覆蓋層218。此外,該裝置結構包含間 隔層250。汲極、源極,閘極、ST1區及間隔係使用傳統 技術形成。 其次,H-R層260係形成於裝置結構上。H-R層係使用傳 統電漿輔助化學氣相沈積法(PECVD)形成*該技術係說明於 Gupta 等人所著的 The Preparation, Properties and Application of Silicon Nitride Thin Films Deposited By Plasraa-Enhanced Chemical Vapor Deposition, Thin SolidFiUs,2(M(1991),在此倂入本案以爲參考資料。執 行PECVD的溫度通常在大約300 -500 eC間。電子迴旋加速 器共振式化學氣相沈積(ECRCVD)技術係用以形成該H-R層 。ECRCVD技術係說明於Kotecki等人所著的Hydrogen Incorporated In Silicon Nitride Films Deposited By Remote El ect ron-Cyc lot ron-Resonance. Cheraica1 Vapor * I . i -9- :, (請先閱讀背面之注意事通 Ϋ寫本頁)
本紙張尺度適用中國國家標隼(CNS ) A4现格(2〗0 X 297公釐) 厂:: 4 57t A 7 B7 五、發明説明(名)
Deposition, J.AppI. Phys.77(3)(Feb. 1,1995),在此倂 入本案以爲參考資料。 該H-R層包含較傳統LPCVD氮化矽更高比例的氫。在一 實施例中,氫比例係大於5%並小於或等於3 9¾。超過大約 3 9%的氫會使氮化矽膜性質劣化,諸如其作爲阻障的能力 。氫比例最好在大約1 0 · 3 5 %間|大約1 2 5 %更佳,大約 12-2 5%則更好,而最好爲15-20%。. 如上述,H-R層的PECVD係於大約300 -5 0(TC間的溫度執 行。在較低溫下形成該Η - R層係爲有利的。例如,Η - R層 的氮原子將於後續執行溫度較PECVD溫度爲高的製程期間 ,擴散通過裝置結構。在部份案例中,後續的較高溫製.程 係足以鈍化表面狀態,而無須鈍化退火。經鈍化的表面狀 態係以“ + "表示。 鈍化退火可用以鈍化表面狀態。傳統鈍化退火通常係於 大約400 °C的氫氣或氫氣/氮氣(形成氣體)氣氛中執行 大約30- 60分鐘。然而,使用H-R層將提供即時的氫源, 經濟部中央橾準局I工消費合作社印製 {請先閲讀背面之注$項If A寫本頁) 因而減少或消除對於含氫退火的需求,以有效地鈍化表而 狀態。 參考第3圖,一 H-R層315係形成部份的閘極結構,以鈍 化表面狀態。如所示,該H-R層315係形成於複合閘極310 的矽化物層314與氮化矽覆蓋層318間》H-R層315可單獨 使用或與如第2圖所述之H-R層260共用。額外的H-R層或 諸層可被形成於裝置中,以增強表面狀態的鈍化。 · 1 ·-...... .
m I -ίο- ' ! 本紙張尺度適用中國國家榡卒(CNS ) A4規格(210X297公釐) ί 4575; A7 B7 五、發明説明(q ) 在該H-R氮化矽層沈積於諸如鎢柱結構或矽化鎢複合閘 極等鎢層的應用中,一黏著性改良層係爲所需。該黏著性 改良層因氮化物通常無法緊密地黏著於鎢而爲所需。爲改 良鎢與氮化物間的黏著性,一薄矽層係於H-R層沈積前形 成於錫上? 在另一實施例中,但氮氧化物係用於取代H-R氮化矽’ 以做爲諸如阻障層等鈍化結構。該氮氧化物係以諸如電漿 輔助化學氣相沈積法(PECVD)沈積》以PECVD沈積氮氧化物 係說明於Habraken與Kuiper等人所著的“ Silicon Nitride and Oxynitride Films , Material Science and E n g i n e e r i n g,R 1 2 N o . 3,J u 1 y 1 9 9 4 , p p . 1 2 3 1 7 5,在此 併入本案以爲參考資料。諸如矽烷(SiH4)、氨氣(NH3)和/ 或氮氣(N2)及氧化亞氮(N20)等預製體將引入反應器中以 形成氮氧化物層,該氮氧化物的沈積.條件係爲諸如大約300 - 1000W的功率,大約2-10 Torr的壓力及大約300,500 t 的溫度。該氮氧化物的沈積條件最好爲諸如大約300 - 800W 的功率、大約2-6 Tor r的壓力及大約350 -480 °C的溫度· 經濟部中央標準局負工消費合作社印裝 (請先閱讀背面之注意事項〖<寫本頁) 在一實施例中* PECVD係於諸如Applied Materials公 司所製造的ΑΜΕ 5000單晶圓設備中執行*或著諸如 Novellus System 公司所製造的 Novellus Concept-Ι 多站 晶圓設備中執行。該單晶圓與多站晶圓設備用的典型製程 條件係表示於表1中6當然h些參數可爲特定的設備或製 程而做最佳化。 -11- i 本紙张尺度適用中國國家標隼(CNS )八4現格(210X29"?公釐) 45/555 Α7 Β7 五、發明説明(丨ο ) 表1實驗 單 晶圓加工製程條件 含 2 ft矽烷的氮氣流量 :3000sccra NH3流量:15 sccra N20流量:10-40 sccra(將改變氧氣含量) 流量:1050-1020 sccra n2 +n2o總流量定値爲 1060 seem 功 率:3 4 0 w a t t s 溫 度:4 8 0。。 間 隔:3 50 - 380 rai Is 壓 力:5 . 7 5 t 0 r r (請先閱讀背面之注意^5.-it·寫本頁) 多站加工 製程條件 矽院流量 • 0.15 s1m nh3流量 :1 . 8 s 1 ra N2o流量 :0 2-2 s 1m(將改變氧氣含量) N2流量: 11.8-10 si !L n2+n2o總流量定値爲 12 ε 1 ra 功率:0 . 7 Itw(HF)及 0.10kw(LF ) 溫度:4 0 0 t 壓力:5 . 7 5 t 〇 r r 經濟部中央標隼局貝工消费合作社印製 此外,該氣氮化物係以LPCVD沈積。LPCVD氮氧化物的 典型製程條件係表示於表2中。當然這些參數可爲特定的 加工或製程而做最佳化。 表2 _ 典型製程條件 -LPCVD氮氧化物 二氯矽烷的流 量:135 seem Ν Η 3流量:9〇 seem Ν 2流量· 4 5 〇 seem 溫度:77 0 °C 壓力:2 50 ni t 0 r r -12- 本紙張又度適用中國國家標準(CNS ) A4規格(公釐) 5 7 5 5 5 A7 B7 五、發明説明(丨丨) 形成保護層後,將裝置結構退火以鈍化表面狀態。該退 火係於諸如含氫氣氛中進行*此外’該退火可被整合爲部 份的後續製程。 使用該氮氧化物層作爲阻障襯墊時將產生極低的N與P 擴散之可再現性STI接合接面漏電流°參考第5Α·Β圖,其 係由單晶圓及多站晶圓加工所製作之氮氧化物的STI接合 接面漏電流(意指NL,ND與PD周邊漏電流)與折射係數 的關係圖。如所示,漏電流係相當低’由單站加工所形成 的氮氧化物係低於1.4 namps而由多站加工所形成的氧氛 化物係低於0.9 namps 。此外,使用氮氧化物作爲阻障保 護層將使同一批或不同批的晶圓間的漏電流分佈相當均.勻 b 經濟部中央標準局貝工消费合作杜印製 (讀先閲讀背面之注意事名填寫本頁} 如第8圖所示,其已發現吸附於H-R氮化物與氮氧化物 膜中之矽<SiH或SiH/<SiH + NH)的氫比例與接面漏電流的 關係。其已發現較低比例之氫對矽的吸附將降低接面漏電 流,而較高的比例將增加接面漏電流。氫吸附於矽的比例 與接面漏電流間的關係指出較低比例的S i Η或 SiH/(SiH + NH)將改良鈍化結構的鈍化特性。其確信較低比 例將使氫較易穿透該鈍化結構,因而允許氣氛中的氫穿過 並鈍化表面狀態β此外,其確信較低比例的S i Η將降低膜 的電子捕捉,因而改良其漏電特性《詳閱Smith所著之“ Controlling the plasma chemistry of silicon nitride and oxide deposition from silane ’ J . V a c . S c i . Tech.,. -13- ' 本紙張尺度適用中國國家標準(CNS ) A4規格(210>〇97公釐) ~~' 457555 Α7 Β7 五、發明説明(丨l )
An(4)Jul/Aug, 1 993 P1 843,在此併入本案以爲參考資 料"所以,該鈍化結構將形成具有較高或更均勻遲滯時間 的記憶晶片。在一實施例中,S i Η的比例大約爲0 - 3 9 %,最 好爲大約3 - 2(Η,而3 - 8¾則更佳。 在部份應用中,該阻障層係作爲蝕刻阻絕,諸如用於形 成無邊際接觸《在該應用中|諸如硼磷矽酸鹽玻璃(BPSG) 或其他氧化物等中間介電質對氧氮.化物的選擇性或蝕刻速 率比例應夠高,而使該氮氧化物可作爲蝕刻阻絕。第4圖 係繪製使用氟碳化學物質之氮氧化膜對氧化物的選擇性》 線41代表在多站晶圓加工中所形成的氮氧化物,而線42 代表在單晶圓加工中所形成的氮氧化物。對多站晶圓加工 而言,該氮氧化物選擇性範圍係由折射係數1.66時的13:1 至折射係數爲1.9時的24:1。對單晶圓加工而言*該氮氧 化物選擇性範圍係由折射係數1 . 7 1時的1 3 : 1至折射係數 爲1 . 98時的29 : 1。該選擇性係足以使該氮氧化物作爲蝕 刻阻絕。特定應用所選擇的實際選擇性係取決於諸如設計 參數。 經濟部中央標準局員工消费合作社印裝 (請先閲讀背面之注意事¾讲寫本頁) 在ND,PD及NL裝置中量測STI接合接面漏電流的實驗 係使用由具有STI梳狀周邊的擴散盤曲管所組成之巨構'予 以執行。0 . 2um的擴散間距係被提供,且該STI係以閘極 導體覆蓋。該擴散線寬係爲大約0 . 55urn,且該GC梳狀物 係爲大約2 . 5um寬。盤曲管長度係爲大約58400ura,而形 成具有32〗20umz之面積的周邊長1 16800um。第5A圖係:繪. -14- 本紙張尺度適用中國國家榡车i CNS )八4洗格(210X297公釐} 457555 A7 B7 五、發明説明(15 ) 製爲形成於單晶圓加工中之氧氮化物折射係數之函數的NL * ND及PD漏電流*而第5B圖係繪製爲形成於多站加工中 之氧氮化物折射係數之函數的ML,ND及PD漏電流。如所 示’具有1.7-1.9折射係數之形成於單晶圓加工中之氧氮 化物的裝置的漏電流係小於1 . 5 namp,而具有1 . 66 - 1 . 9 折射係數之形成於多站晶圓加工中之氮氧.化物的裝置的漏 電流係小於1 n a no p。 範例1 經濟部中央標準局貝工消費合作社印製 (請先閲績背面之注意升填寫本頁) 進行一實驗以比較具有H-K氮化矽層之裝置與具有傳統 氮化矽層之裝置的漏電流。具有裝置製造於其上的八組試 件(試件A - Η )係被製備。該八組試件係以二種不同的方法 加工。A - D組試件包含以傳統LPCVD氮化矽層所製造的裝 罝結構,該氮化矽係作爲裝置互連界面的阻障或襯墊層。 在A-D組試件中的裝置結構係類似於第1圖所述者。該傳 統LPCVD氮化矽膜係藉由氨(NH3)與二氯矽烷(SicUH2)在 大約720 °C與200 raTorr的爐中反應而被沈積-NH3對 SiCl2H2的比例係爲大約10 : 1。在E-Η組試件,該LPCVD氮 化物層係以H-R氮化矽層取代,諸如第2圖所述者。該H-R 層係於大約480 °C、5.75 Torr與340 Watts之反應器中以 PECVD法沈積。反應物的製程參數如下:大約3000 seem 之包含2%砂院的氮氣、大約1060sccra的氣氣及大約!5sccra 的 NH;。 二組試件的漏電流係使用SZE所著之Physics - j 15- : 本紙張尺度適用中國國家標準(cns )A4現格(210x297公釐) 4 5 7 5 5 5 A7 B7 五、發明説明(/4 ) S e m i c ο n d u c t 〇 r D e v i c e s,W i 1 e y ( 1 9 6 9 )中所述的標準接面 漏電流測試法,在此倂入本案以爲參考資料。參考第6圖 ’各組試件之ST I接合接面漏電流測試係以任意尺度表示 ° A-D組試件代表具有LPCVD氮化物層的晶圓,而E-Η組試 件代表具有LPCVD H-R氮化物層的晶圓。具有傅統LPCVD 氮化物層的試件明顯地較具有PECVD H-R氮化矽層的試件 有更高的漏電流。 範例2 經濟部中央標準扃貝工消費合作社印焚 (請先閲讀背面之注意事«.填寫本頁) 在第7圖中,PEC VD Η · R氮化物膜(試件A · C)的特性係與 LPCVD氮化物膜做比較。試件A係爲在NovellusConcept-1 係統中以PECVD法所沈積的標準氮化矽。試件b係爲在 Novellus Concept-Ι系統中所沈積的低SiH/UV PECVD氮化 物膜。二試件A與B係於Novellus所要求的相似條件下形 成’如 “ Users guide to 200ram PECVD processing for the Novellus Concept One - 200rara Dielectric System n (爲 Novellus System, Inc.,of San Jose, CA.1 992 )所述,在 此倂入本案以爲參考資料。試件C係爲於Appl i ed Materials of Santa Clara, CA 所製造的 ΑΜΕ 5000 系統中 ,以PECVD法沈積的Η _ R氮化矽膜,其作業條件係與試件1 的PECVD氮化物膜(E-Η)相似。試件D係爲以LPCVD法所沈 積的LPCVD氮化物膜*其作業條件係與試件1的LPCVD膜 (A - D )相似* 形成該膜後,該試件係被加熱至720 °C。,參考第.7圖, -16- :; Λ紙張尺度適用中國國家標隼(CNS > A4規格(2l〇x297公釐) 45755 A7 B7 五、發明説明(π ) 試件的氫含量係於試件被加熱至7 20 °C後量測。由第7圖 觀之,在加熱至720 °C後,PECVD H-R膜的氫含量(試件 A-C )將減少,而LPCVD氮化物膜(試件D)僅微量或無 變化。此舉證明Η - R層係有效地提供氫以鈍化表面狀態。 範例3 進行一實驗以分析SiH/(SiH + NH)與ND周邊漏電流間之 關係’其係使用與第5A-B圖相似的巨模。實驗數據係繪製 成第8圖。由第8圖明顯地看出,較低的氧氮化物膜SiH/ (SiH + NH)濃度將產生較低的ND周邊漏電流。在SiH/(SiH + NH) 濃度大約爲0 - 3 5%時,該ND漏電流的範圍則大約爲〇 . 63 narop 至 1.72 narop ° 經濟部中央榇隼局貞工消費合作社印製 (讀先閲讀背面之注意事ί ‘填寫本頁) 雖然本發明已被特別地揭示並參考不同的實施例做說明 ,但在不違背本發明之範嗦下對本發明所做的改良與改變 將可爲熟習本技藝之人士所辨別。例如,該鈍化層可作爲 一單一膜閫極介電質覆蓋物、包含諸如LPCVD氮化物和/ 或各種氧化物膜等其他膜的一複合閘極覆蓋物、單獨使用 或與其他介電材料結合之作爲最終晶片鈍化材料的閘極導 體間隔膜、移動離子和/或金屬污染物阻絕或一接觸蝕刻 阻絕。因此,本發明之範疇並非取決於參考上述說明,而 係取決於參考所附之申請專利範圍與其所有相當的範_。 主要元件之對照表: 100 基板 101 DRAM 單元 v
I -17- !
I 本纸張尺度速用中國國家標準(CNS ) A4规格(210X 297公釐) 4575 A7 B7 五、發明説明( A ) 經濟部中央標準局員工消費合作社印製 105 電 容 器 106 電 晶 體 110 閘 極 111 閘 極 氧 化 物 112 多 晶 矽 114 矽 化 物 116 氮 化 物 覆 蓋 120 源 極 130 汲 極 140 淺 溝 渠 隔 魁 離 160 間 隔 170 氛 化 物 層 200 裝 匱 結 構 210 閘 極 212 多 晶 矽 層 214 砂 化 物 層 218 氮 化 矽 覆 蓋 層 230 源 極 240 ST1區 250 間 隔 層 260 -ΜΞ 墊 層 310 複 合 閘 極 314 矽 化 物 層 3 15 Η - R層 318 氮 化 矽 覆 蓋 層 -18- 本紙張尺度適用中國國家椋準< CNS ) A4規格(210X297公釐) P I . . ί I—~、τ~_ —i : (請先閲讀背面之注意事这 填寫本頁) ί
Claims (1)
- A8 BS CS D8 4 5 7 5 5 六、申請專利範圍 第88 103302號「利用氮氧化矽之表面鈍化」專利案 (90年6月修正) 六申請專利範圍: 1. 一種在半導體裝置製造中,用於在裝置中易於鈍化表 面狀態的製程,其包含的步驟爲: 形成包含有氮氧化矽層的一鈍化層於裝置中;以及 在氫氣氣氛中加熱該裝置,使該氮氧化矽層含豐富氫 以鈍化表面狀態而減少漏電流。 ---------:---'裝--------訂--------線 ί 一 (請先閱讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 本紙張尺度遇用中阀囡家楳準(CNS)A4規格(2〗0 X ;W公《 )
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US10756084B2 (en) | 2015-03-26 | 2020-08-25 | Wen-Jang Jiang | Group-III nitride semiconductor device and method for fabricating the same |
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1999
- 1999-03-04 TW TW088103302A patent/TW457555B/zh not_active IP Right Cessation
- 1999-03-09 EP EP99301756A patent/EP0942464A3/en not_active Withdrawn
- 1999-03-09 KR KR1019990007722A patent/KR100633191B1/ko not_active IP Right Cessation
- 1999-03-09 JP JP11061799A patent/JPH11317404A/ja active Pending
- 1999-03-09 CN CNB991031210A patent/CN1171289C/zh not_active Expired - Fee Related
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2000
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TWI572034B (zh) * | 2015-03-26 | 2017-02-21 | wen-zhang Jiang | III / nitride semiconductor device and method for producing the same |
US10756084B2 (en) | 2015-03-26 | 2020-08-25 | Wen-Jang Jiang | Group-III nitride semiconductor device and method for fabricating the same |
US11335799B2 (en) | 2015-03-26 | 2022-05-17 | Chih-Shu Huang | Group-III nitride semiconductor device and method for fabricating the same |
Also Published As
Publication number | Publication date |
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EP0942464A3 (en) | 2000-07-26 |
KR19990077708A (ko) | 1999-10-25 |
CN1242597A (zh) | 2000-01-26 |
CN1171289C (zh) | 2004-10-13 |
JPH11317404A (ja) | 1999-11-16 |
EP0942464A2 (en) | 1999-09-15 |
KR100633191B1 (ko) | 2006-10-11 |
US6483172B1 (en) | 2002-11-19 |
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