US20160307776A1 - Method for manufacturing semiconductor device - Google Patents
Method for manufacturing semiconductor device Download PDFInfo
- Publication number
- US20160307776A1 US20160307776A1 US15/198,131 US201615198131A US2016307776A1 US 20160307776 A1 US20160307776 A1 US 20160307776A1 US 201615198131 A US201615198131 A US 201615198131A US 2016307776 A1 US2016307776 A1 US 2016307776A1
- Authority
- US
- United States
- Prior art keywords
- film
- oxide semiconductor
- insulating film
- semiconductor film
- gate insulating
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000004065 semiconductor Substances 0.000 title claims abstract description 197
- 238000000034 method Methods 0.000 title abstract description 22
- 238000004519 manufacturing process Methods 0.000 title abstract description 19
- 239000001257 hydrogen Substances 0.000 claims description 37
- 229910052739 hydrogen Inorganic materials 0.000 claims description 37
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 34
- 229910052760 oxygen Inorganic materials 0.000 claims description 34
- 239000001301 oxygen Substances 0.000 claims description 34
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 33
- 238000010438 heat treatment Methods 0.000 claims description 22
- 230000002950 deficient Effects 0.000 claims description 9
- 229910052733 gallium Inorganic materials 0.000 claims description 7
- 229910052738 indium Inorganic materials 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- 239000000758 substrate Substances 0.000 abstract description 76
- 230000008021 deposition Effects 0.000 abstract description 14
- 239000010408 film Substances 0.000 description 283
- 239000007789 gas Substances 0.000 description 87
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 26
- 239000010409 thin film Substances 0.000 description 26
- 239000010410 layer Substances 0.000 description 21
- 229910052710 silicon Inorganic materials 0.000 description 19
- 239000010703 silicon Substances 0.000 description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- 229910052581 Si3N4 Inorganic materials 0.000 description 18
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 18
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 17
- 229910007541 Zn O Inorganic materials 0.000 description 15
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 14
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 14
- 239000012535 impurity Substances 0.000 description 14
- 238000004544 sputter deposition Methods 0.000 description 14
- 229910052782 aluminium Inorganic materials 0.000 description 13
- 238000000151 deposition Methods 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 12
- 230000002349 favourable effect Effects 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 239000010936 titanium Substances 0.000 description 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 9
- 230000004888 barrier function Effects 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 229910052719 titanium Inorganic materials 0.000 description 9
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 8
- 239000012298 atmosphere Substances 0.000 description 8
- 238000010586 diagram Methods 0.000 description 8
- 229910052814 silicon oxide Inorganic materials 0.000 description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 7
- 229910052786 argon Inorganic materials 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 7
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 7
- 229910052750 molybdenum Inorganic materials 0.000 description 7
- 239000011733 molybdenum Substances 0.000 description 7
- 229910052721 tungsten Inorganic materials 0.000 description 7
- 239000010937 tungsten Substances 0.000 description 7
- 239000011787 zinc oxide Substances 0.000 description 7
- 239000000956 alloy Substances 0.000 description 6
- 239000001307 helium Substances 0.000 description 6
- 229910052734 helium Inorganic materials 0.000 description 6
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 6
- 229910044991 metal oxide Inorganic materials 0.000 description 6
- 150000004706 metal oxides Chemical class 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 5
- 238000005530 etching Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 238000004151 rapid thermal annealing Methods 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 239000012300 argon atmosphere Substances 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 4
- 229910052754 neon Inorganic materials 0.000 description 4
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 4
- 150000004767 nitrides Chemical class 0.000 description 4
- 229960001730 nitrous oxide Drugs 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000002356 single layer Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910019092 Mg-O Inorganic materials 0.000 description 3
- 229910019395 Mg—O Inorganic materials 0.000 description 3
- 229910052779 Neodymium Inorganic materials 0.000 description 3
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 229910003437 indium oxide Inorganic materials 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 235000013842 nitrous oxide Nutrition 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- -1 tungsten nitride Chemical class 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- 229910000846 In alloy Inorganic materials 0.000 description 2
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 2
- 229910021417 amorphous silicon Inorganic materials 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001678 elastic recoil detection analysis Methods 0.000 description 2
- QZQVBEXLDFYHSR-UHFFFAOYSA-N gallium(III) oxide Inorganic materials O=[Ga]O[Ga]=O QZQVBEXLDFYHSR-UHFFFAOYSA-N 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 2
- 229920005591 polysilicon Polymers 0.000 description 2
- 238000005036 potential barrier Methods 0.000 description 2
- 239000003870 refractory metal Substances 0.000 description 2
- 238000005001 rutherford backscattering spectroscopy Methods 0.000 description 2
- 229910052706 scandium Inorganic materials 0.000 description 2
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 description 2
- 229910052990 silicon hydride Inorganic materials 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910020923 Sn-O Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910000611 Zinc aluminium Inorganic materials 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- HXFVOUUOTHJFPX-UHFFFAOYSA-N alumane;zinc Chemical compound [AlH3].[Zn] HXFVOUUOTHJFPX-UHFFFAOYSA-N 0.000 description 1
- 239000005407 aluminoborosilicate glass Substances 0.000 description 1
- 239000005354 aluminosilicate glass Substances 0.000 description 1
- JYMITAMFTJDTAE-UHFFFAOYSA-N aluminum zinc oxygen(2-) Chemical compound [O-2].[Al+3].[Zn+2] JYMITAMFTJDTAE-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- AJNVQOSZGJRYEI-UHFFFAOYSA-N digallium;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Ga+3].[Ga+3] AJNVQOSZGJRYEI-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910001195 gallium oxide Inorganic materials 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-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
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- 238000007500 overflow downdraw method Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 229910001256 stainless steel alloy Inorganic materials 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 description 1
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—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
- H01L21/34—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 not provided for in groups H01L21/0405, H01L21/0445, H01L21/06, H01L21/16 and H01L21/18 with or without impurities, e.g. doping materials
- H01L21/44—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/38 - H01L21/428
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
- C23C16/308—Oxynitrides
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45563—Gas nozzles
- C23C16/45578—Elongated nozzles, tubes with holes
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/50—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges
- C23C16/511—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges using microwave discharges
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32009—Arrangements for generation of plasma specially adapted for examination or treatment of objects, e.g. plasma sources
- H01J37/32192—Microwave generated discharge
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32431—Constructional details of the reactor
- H01J37/3244—Gas supply means
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32431—Constructional details of the reactor
- H01J37/3244—Gas supply means
- H01J37/32449—Gas control, e.g. control of the gas flow
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/34—Gas-filled discharge tubes operating with cathodic sputtering
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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
- H01L21/02225—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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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
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Definitions
- the present invention relates to a semiconductor device and a method for manufacturing the semiconductor device.
- the present invention particularly relates to a semiconductor device including an oxide semiconductor and a method for manufacturing the semiconductor device. Further, the present invention relates to an apparatus used for manufacturing a semiconductor device.
- a thin film transistor including a semiconductor film formed over an insulating surface is an essential semiconductor element for a semiconductor device. Since there is limitation on the allowable temperature limit of a substrate in manufacture of a thin film transistor, a thin film transistor in which amorphous silicon that can be deposited at a relatively low temperature, polysilicon that can be obtained by crystallization with use of laser light or a catalytic element, or the like is included in an active layer is mainly used for a semiconductor display device.
- a metal oxide having semiconductor characteristics which is referred to as an oxide semiconductor has attracted attention as a novel semiconductor material which has both high electron mobility, which is a characteristic of polysilicon, and uniform element characteristics, which is a characteristic of amorphous silicon.
- the metal oxide is used for various applications.
- indium oxide is a well-known metal oxide and used as a material of a transparent electrode included in a liquid crystal display device or the like.
- metal oxides having semiconductor characteristics include tungsten oxide, tin oxide, indium oxide, and zinc oxide.
- Thin film transistors in which a channel formation region is formed using such a metal oxide having semiconductor characteristics are known (Patent Documents 1 and 2).
- a transistor used for a semiconductor device is required to have favorable transistor characteristics such as on current, off current, and electron mobility.
- the semiconductor device can be driven at higher speed.
- a highly reliable semiconductor device can be provided.
- the purity of an oxide semiconductor used in a channel formation region of a transistor is increased and the quality of a gate insulating film which is in contact with the oxide semiconductor is improved.
- an i-type or substantially i-type oxide semiconductor a highly purified oxide semiconductor which is obtained by removal of an impurity is extremely sensitive to an interface state or an interface charge; therefore, the conditions of a gate insulating film and the interface between the gate insulating film and an oxide semiconductor film need to be kept favorable.
- oxide semiconductor film In order to increase the purity of the oxide semiconductor, it is necessary to remove, from the oxide semiconductor, hydrogen that serves as a donor in the oxide semiconductor and becomes a factor causing the oxide semiconductor to be an n-type oxide semiconductor. Then, oxygen is supplied to a deficient portion from which hydrogen is removed and oxygen is supplied to compensate oxygen which is lost at the same time as the removal of hydrogen, whereby the oxide semiconductor film is highly purified.
- a dense insulating film having few defects is used as the gate insulating film which is in contact with the highly purified oxide semiconductor film.
- the defect here refers to a dangling bond or the like in the gate insulating film.
- An embodiment of the present invention is a method for manufacturing a semiconductor device which includes a gate electrode, an oxide semiconductor film, and a gate insulating film that is formed using a high-density plasma CVD apparatus, including the steps of: setting a substrate to face a dielectric plate provided in a reaction chamber of the high-density plasma CVD apparatus; ejecting a gas for generating plasma toward the dielectric plate to generate plasma; and ejecting a source gas of the gate insulating film toward the substrate, so that the gate insulating film is formed.
- Another embodiment of the present invention is a method for manufacturing a semiconductor device which includes a gate electrode, an oxide semiconductor film, and a gate insulating film that is formed using a high-density plasma CVD apparatus, including the steps of: setting a substrate to face a dielectric plate provided in a reaction chamber of the high-density plasma CVD apparatus; ejecting a gas for generating plasma toward the dielectric plate from a first gas pipe to generate plasma; and ejecting a source gas of the gate insulating film toward the substrate from a second gas pipe which is provided to intersect with the first gas pipe, so that the gate insulating film is formed.
- Another embodiment of the present invention is a method for manufacturing a semiconductor device which includes a gate electrode, an oxide semiconductor film, and a gate insulating film that is formed using a high-density plasma CVD apparatus, including the steps of: setting a substrate to face a dielectric plate provided in a reaction chamber of the high-density plasma CVD apparatus; ejecting a gas for generating plasma toward the substrate to generate plasma; and ejecting a source gas of the gate insulating film toward the substrate, so that the gate insulating film is formed.
- Another embodiment of the present invention is a method for manufacturing a semiconductor device which includes a gate electrode, an oxide semiconductor film, and a gate insulating film that is formed using a high-density plasma CVD apparatus, including the steps of: setting a substrate to face a dielectric plate provided in a reaction chamber of the high-density plasma CVD apparatus; ejecting a gas for generating plasma toward the substrate from a member provided in parallel with the dielectric plate to generate plasma; and ejecting a source gas of the gate insulating film toward the substrate from a gas pipe which is provided to intersect with the member, so that the gate insulating film is formed.
- the characteristics of the interface between an oxide semiconductor film and the gate insulating film can be improved.
- the transistor characteristics such as on current, off current, electron mobility, and reliability become favorable; accordingly, a semiconductor device can operate at high speed and the reliability thereof can be improved.
- FIGS. 1A to 1E are cross-sectional views of a semiconductor device
- FIG. 2 is a top view of a manufacturing apparatus
- FIG. 3 is a cross-sectional view of a manufacturing apparatus
- FIG. 4 is a flow chart
- FIG. 5 is a cross-sectional view of a manufacturing apparatus
- FIG. 6 is a cross-sectional view of a semiconductor device
- FIG. 7 is a cross-sectional view of a semiconductor device
- FIG. 8 is a cross-sectional view of a semiconductor device
- FIGS. 9A to 9E illustrate examples of electronic devices
- FIGS. 10A and 10B show characteristics of transistors
- FIGS. 11A and 11B show characteristics of transistors
- FIG. 12 is a longitudinal sectional view of a bottom-gate thin film transistor including an oxide semiconductor
- FIGS. 13A and 13B are energy band diagrams (schematic diagrams) along a section A-A′ in FIG. 12 ;
- FIG. 14A illustrates the state where a positive potential (+VG) is applied to a gate (G 1 ), and 14 B illustrates the state where a negative potential ( ⁇ VG) is applied to the gate (G 1 );
- FIG. 15 illustrates relations between the vacuum level and the work function of a metal ( ⁇ M) and between the vacuum level and the electron affinity ( ⁇ ) of an oxide semiconductor
- FIG. 16 is a plan view of a manufacturing apparatus.
- a method for manufacturing a semiconductor device will be described with reference to FIGS. 1A to 1E by taking a bottom-gate thin film transistor having a channel-etched structure as an example.
- a gate electrode 101 is formed over a substrate 100 .
- the substrate 100 the following can be used: an alkali-free glass substrate manufactured by a fusion method or a floating method, such as a barium borosilicate glass substrate, an aluminoborosilicate glass substrate, or an aluminosilicate glass substrate; a ceramic substrate; a plastic substrate with heat resistance enough to withstand a process temperature in this manufacturing process; or the like.
- a metal substrate such as a stainless steel alloy substrate having a surface provided with an insulating layer may be used.
- An insulating film serving as a base film may be formed between the substrate 100 and the gate electrode 101 .
- a single layer of a silicon oxide film, a silicon oxynitride film, a silicon nitride film, a silicon nitride oxide film, an aluminum nitride film, or an aluminum nitride oxide film or a stacked layer of a plurality of these films can be used.
- an insulating film with a high barrier property such as a silicon nitride film, a silicon nitride oxide film, an aluminum nitride film, or an aluminum nitride oxide film
- impurities in an atmosphere such as moisture or hydrogen, or impurities included in the substrate 100 such as alkali metal or heavy metal can be prevented from entering an oxide semiconductor film, a gate insulating film, an interface between the oxide semiconductor film and the gate insulating film or the like, or the vicinity of the interface.
- oxynitride refers to a substance which includes more oxygen than nitrogen
- nitride oxide refers to a substance which includes more nitrogen than oxygen
- silicon oxynitride is a substance including oxygen, nitrogen, silicon, and hydrogen in the ranges of greater than or equal to 50 atomic % and less than or equal to 70 atomic %, greater than or equal to 0.5 atomic % and less than or equal to 15 atomic %, greater than or equal to 25 atomic % and less than or equal to 35 atomic %, and greater than or equal to 0.1 atomic % and less than or equal to 10 atomic %, respectively.
- silicon nitride oxide is a substance including oxygen, nitrogen, silicon, and hydrogen in the ranges of greater than or equal to 5 atomic % and less than or equal to 30 atomic %, greater than or equal to 20 atomic % and less than or equal to 55 atomic %, greater than or equal to 25 atomic % and less than or equal to 35 atomic %, and greater than or equal to 10 atomic % and less than or equal to 30 atomic %, respectively.
- the above ranges are obtained by measurement using Rutherford backscattering spectrometry (RBS) or hydrogen forward scattering spectrometry (HFS).
- the total of the percentages of the constituent elements does not exceed 100 atomic %.
- the gate electrode 101 can be formed using a single layer or a stacked layer of one or more conductive films including a metal material such as molybdenum, titanium, chromium, tantalum, tungsten, neodymium, or scandium, or an alloy material which includes any of these metal materials as a main component; or a nitride of any of these metals.
- a metal material such as molybdenum, titanium, chromium, tantalum, tungsten, neodymium, or scandium, or an alloy material which includes any of these metal materials as a main component; or a nitride of any of these metals.
- aluminum or copper can also be used as the above metal material as long as it can withstand the temperature of heat treatment performed in a later step.
- Aluminum or copper is preferably used in combination with a refractory metal material in order to avoid problems of heat resistance and corrosion.
- the following structures are preferable: a two-layer structure in which a molybdenum film is stacked over an aluminum film; a two-layer structure in which a molybdenum film is stacked over a copper film; a two-layer structure in which a titanium nitride film or a tantalum nitride film is stacked over a copper film; and a two-layer structure in which a titanium nitride film and a molybdenum film are stacked.
- the following structure is preferable: a stacked-layer structure including an aluminum film, an alloy film of aluminum and silicon, an alloy film of aluminum and titanium, or an alloy film of aluminum and neodymium in a middle layer and any of a tungsten film, a tungsten nitride film, a titanium nitride film, and a titanium film in a top layer and a bottom layer.
- the aperture ratio of a pixel portion can be improved.
- the gate electrode 101 is formed to a thickness of 10 nm to 400 nm, preferably 100 nm to 200 nm
- a conductive film for the gate electrode is formed to a thickness of 150 nm by a sputtering method using a tungsten target, and then the conductive film is processed (patterned) into a desired shape by etching; thus, the gate electrode 101 is formed.
- a gate insulating film 102 is formed over the gate electrode 101 .
- the gate insulating film 102 is preferably formed by deposition treatment using high-density plasma. With high-density plasma, plasma damage to the gate insulating film 102 can be reduced. Accordingly, dangling bonds in the gate insulating film 102 can be reduced and defects can be reduced; thus, the interface with an oxide semiconductor formed later can be highly favorable.
- the gate insulating film 102 can be formed to have a single-layer or stacked-layer structure with use of any of materials such as a silicon oxide film, a silicon nitride film, a silicon oxynitride film, and a silicon nitride oxide film.
- a silicon oxynitride film is formed using silane and nitrogen monoxide as a deposition gas.
- the thickness of the gate insulating film 102 is greater than or equal to 100 nm and less than or equal to 500 nm
- a first gate insulating film with a thickness of greater than or equal to 50 nm and less than or equal to 200 nm and a second gate insulating film with a thickness of greater than or equal to 5 nm and less than or equal to 300 nm are stacked in this order.
- the gate insulating film 102 can be formed by stacking a silicon oxide film or a silicon oxynitride film, and a silicon nitride film or a silicon nitride oxide film in this order from the substrate side.
- the gate insulating film 102 can be formed by stacking a silicon nitride film or a silicon nitride oxide film, a silicon oxide film or a silicon oxynitride film, and a silicon nitride film or a silicon nitride oxide film in this order from the substrate side.
- a 100-nm-thick silicon oxynitride film is formed by plasma CVD using microwaves of 2.45 GHz as high-density plasma.
- a microwave refers to a wave in the frequency range of 300 MHz to 300 GHz.
- dust attached to a surface of the gate insulating film 102 is preferably removed by reverse sputtering in which an argon gas is introduced and plasma is generated.
- the reverse sputtering refers to a method in which, without application of voltage to a target side, an RF power source is used for application of voltage to a substrate side in an argon atmosphere so that plasma is generated in the vicinity of the substrate to modify a surface.
- an argon atmosphere a nitrogen atmosphere, a helium atmosphere, or the like may be used.
- an argon atmosphere to which oxygen, nitrous oxide, or the like is added may be used.
- an argon atmosphere to which chlorine, carbon tetrafluoride, or the like is added may be used.
- an oxide semiconductor film such as an In—Sn—Ga—Zn—O film, an In—Ga—Zn—O film, an In—Sn—Zn—O film, an In—Al—Zn—O film, a Sn—Ga—Zn—O film, an Al—Ga—Zn—O film, a Sn—Al—Zn—O film, an In—Zn—O film, a Sn—Zn—O film, an Al—Zn—O film, a Zn—Mg—O film, a Sn—Mg—O film, an In—Mg—O film, an In—O film, a Sn—O film, or a Zn—O film can be used.
- the oxide semiconductor film may include SiO 2 .
- a thin film expressed by InMO 3 (ZnO) m (m>0) can be used.
- M represents one or more metal elements selected from Ga, Al, Mn, and Co.
- M is Ga, Ga and Al, Ga and Mn, Ga and Co, or the like.
- An oxide semiconductor film whose composition formula is expressed by InMO 3 (ZnO) m (m>0) where Ga is included as M is referred to as an In—Ga—Zn—O oxide semiconductor, and a thin film of the In—Ga—Zn—O oxide semiconductor is also referred to as an In—Ga—Zn—O-based non-single-crystal film.
- the thickness of the oxide semiconductor film is 10 nm to 300 nm, preferably 20 nm to 100 nm.
- a DC sputtering method is used, the flow rate of argon is 30 sccm, the flow rate of oxygen is 15 sccm, and the substrate temperature is room temperature.
- the oxide semiconductor film is processed (patterned) into a desired shape by etching or the like, so that an island-shaped oxide semiconductor film 103 is formed over the gate insulating film 102 to overlap with the gate electrode 101 .
- the oxide semiconductor film 103 may be subjected to heat treatment in an atmosphere of an inert gas (such as nitrogen, helium, neon, or argon).
- an oxide semiconductor film 104 from which moisture and hydrogen are eliminated is formed.
- rapid thermal annealing (RTA) treatment can be performed in an atmosphere of an inert gas (such as nitrogen, helium, neon, or argon) at a temperature of higher than or equal to 500° C. and lower than or equal to 750° C. (or a temperature lower than or equal to the strain point of the glass substrate) for approximately 1 minute to 10 minutes, preferably at 600° C. for approximately 3 minutes to 6 minutes.
- the timing of the above heat treatment is not limited to after formation of the island-shaped oxide semiconductor film 103 , and the oxide semiconductor film before being processed into the island-shaped oxide semiconductor film 103 may be subjected to the heat treatment.
- the heat treatment may also be performed plural times after the formation of the oxide semiconductor film 104 .
- the carrier concentration can be reduced, preferably to lower than 1 ⁇ 10 14 /cm 3 .
- impurities such as hydrogen which serves as a donor as much as possible in an oxide semiconductor with an energy gap of 2 eV or more, preferably 2.5 eV or more, more preferably 3 eV or more
- the intrinsic carrier concentration thereof can be reduced to lower than or equal to 1.45 ⁇ 10 10 /cm 3 , which is that of silicon, and to approximately 10 ⁇ 7 /cm 3 according to the Fermi-Dirac distribution law.
- heat treatment is performed for 6 minutes in a nitrogen atmosphere in the state where the substrate temperature reaches 600° C.
- a heating method using an electric furnace a rapid heating method such as a gas rapid thermal annealing (GRTA) method using a heated gas or a lamp rapid thermal annealing (LRTA) method using lamp light, or the like can be used.
- GRTA gas rapid thermal annealing
- LRTA lamp rapid thermal annealing
- the temperature rise characteristics are preferably set at higher than or equal to 0.1° C./min and lower than or equal to 20° C./min and the temperature drop characteristics are preferably set at higher than or equal to 0.1° C./min and lower than or equal to 15° C./min.
- the heat treatment it is preferable that moisture, hydrogen, and the like be not included in nitrogen or a rare gas such as helium, neon, or argon. It is preferable that the purity of nitrogen or a rare gas such as helium, neon, or argon which is introduced into a heat treatment apparatus be 6N (99.9999%) or higher, preferably 7N (99.99999%) or higher (that is, the impurity concentration is 1 ppm or lower, preferably 0.1 ppm or lower).
- the heat treatment may be performed in air where the dew point under atmospheric pressure is ⁇ 60° C. or lower and the moisture content is low, instead of an inert gas atmosphere such as a nitrogen atmosphere or a rare gas atmosphere.
- the island-shaped oxide semiconductor film 104 which has been subjected to the heat treatment in an inert gas atmosphere is preferably in an amorphous state, but may be partly crystallized.
- a conductive film 105 used for a source electrode and a drain electrode is formed over the island-shaped oxide semiconductor film 104 .
- the conductive film 105 is preferably formed using a material with low electronegativity, and may be formed using aluminum, magnesium, or the like by a sputtering method. Further, a film of titanium, tungsten, molybdenum, or the like which has low contact resistance with an oxide semiconductor may be formed between the oxide semiconductor film 104 and the conductive film 105 by a sputtering method.
- a film of titanium, tungsten, molybdenum, or the like may be formed over the conductive film 105 by a sputtering method.
- a conductive film having a two-layer or three-layer structure is formed using any of these in combination as appropriate.
- the thickness of the conductive film 105 may be 100 nm to 500 nm.
- the conductive film 105 is processed (patterned) into a desired shape by etching or the like, so that a source electrode 106 and a drain electrode 107 are formed.
- an exposed portion of the island-shaped oxide semiconductor film 104 is partly etched, so that an island-shaped oxide semiconductor film 108 having a groove (a recessed portion) is formed.
- an insulating film 109 is formed so as to cover the source electrode 106 , the drain electrode 107 , and the oxide semiconductor film 108 .
- insulating film 109 As the insulating film 109 , a 200-nm-thick silicon oxide film is formed by a sputtering method.
- the insulating film 109 can have a stacked-layer structure.
- impurities such as hydrogen included in the oxide semiconductor film are removed as much as possible to increase the purify of the oxide semiconductor film, and the interface characteristics with the gate insulating film which is in contact with the oxide semiconductor film are improved.
- how such treatment affects the characteristics of a transistor is described below.
- FIG. 12 is a cross-sectional view illustrating a thin film transistor manufactured in the above manner.
- An oxide semiconductor film (OS) is provided over a gate electrode (G 1 ) with a gate insulating film (GI) interposed therebetween, and a source electrode (S) and a drain electrode (D) are provided over the oxide semiconductor film.
- a back-gate electrode (G 2 ) is further provided in FIG. 12 , the back-gate electrode (G 2 ) is not necessarily provided.
- FIGS. 13A and 13B are energy band diagrams (schematic diagrams) on A-A′ illustrated in FIG. 12 .
- FIG. 13B illustrates the case where a positive potential with respect to the source is applied to the drain (V D >0).
- FIGS. 14A and 14B are energy band diagrams (schematic diagrams) on B-B′ illustrated in FIG. 12 .
- FIG. 14A illustrates an on state in which a positive potential (+VG) is applied to the gate (G 1 ) and carriers (electrons) flow between the source and the drain.
- FIG. 14B illustrates an off state in which a negative potential ( ⁇ VG) is applied to the gate (G 1 ) and minority carriers do not flow.
- FIG. 15 shows relations between the vacuum level and the work function of a metal ( ⁇ M) and between the vacuum level and the electron affinity ( ⁇ ) of an oxide semiconductor.
- a conventional oxide semiconductor is typically an n-type semiconductor, in which case the Fermi level (E F ) is away from the intrinsic Fermi level (Ei) located in the middle of a band gap and is located closer to the conduction band.
- E F Fermi level
- Ei intrinsic Fermi level
- an oxide semiconductor of the present invention is an intrinsic (i-type) or a substantially intrinsic oxide semiconductor which is obtained by removing hydrogen that is an n-type impurity from an oxide semiconductor and purifying the oxide semiconductor so that the oxide semiconductor does not include an impurity other than a main component thereof as much as possible.
- a feature is that a purified i-type (intrinsic) semiconductor or a semiconductor close thereto is obtained not by adding an impurity but by removing an impurity such as hydrogen or water as much as possible. This enables the Fermi level (E F ) to be at the same level as the intrinsic Fermi level (Ei).
- metal with lower electronegativity than hydrogen may be used for a conductive film for the source electrode (S) and the drain electrode (D).
- the oxygen concentration of the oxide semiconductor film (OS) may be increased.
- the concentration of oxygen that is a main component of the oxide semiconductor hydrogen that is an impurity can be removed and the oxide semiconductor can be highly purified.
- Heat treatment for removing hydrogen from the oxide semiconductor film (OS) is also effective.
- an oxide film with high oxygen concentration may be formed as an insulating film 1200 over the oxide semiconductor film (OS).
- Oxygen is supplied from the insulating film 1200 , whereby the oxygen concentration of the oxide semiconductor film (OS) can be increased.
- an effect of extraction of hydrogen in the oxide semiconductor film (OS) by oxygen in the insulating film 1200 is obtained.
- the oxygen concentration of the insulating film 1200 is set higher than the oxygen concentration of the oxide semiconductor film (OS).
- the gate insulating film (GI) includes oxygen
- hydrogen can also be efficiently extracted by the insulating film 1200 by setting the oxygen concentration of the insulating film 1200 higher than the oxygen concentration of the gate insulating film (GI).
- the insulating film 1200 is preferably formed by a sputtering method.
- the oxide semiconductor can be highly purified.
- the hydrogen concentration may be reduced to, when measured by SIMS measurement, 5 ⁇ 10 19 /cm 3 or lower, preferably 5 ⁇ 10 18 /cm 3 or lower, more preferably 5 ⁇ 10 17 /cm 3 or lower.
- the electron affinity ( ⁇ ) is said to be 4.3 eV.
- the work function of titanium (Ti) included in the source electrode and the drain electrode is substantially equal to the electron affinity ( ⁇ ) of the oxide semiconductor. In that case, a Schottky barrier for electrons is not formed at an interface between the metal and the oxide semiconductor.
- a black circle ( ⁇ ) represents an electron, and when a positive potential is applied to the drain, the electron is injected into the oxide semiconductor over the barrier (h) and flows toward the drain.
- the height of the barrier (h) changes depending on the gate voltage and the drain voltage; in the case where a positive drain voltage is applied, the height of the barrier (h) is smaller than the height of the barrier in FIG. 13A where no voltage is applied, i.e., 1 ⁇ 2 of the band gap (Eg).
- the oxide semiconductor does not include an impurity other than a main component thereof as much as possible, an intrinsic (i-type) or substantially intrinsic oxide semiconductor is obtained. Consequently, the interface characteristics with the gate insulating film become apparent. Therefore, the interface characteristics need to be considered separately from bulk characteristics.
- an insulating film formed using high-density plasma is preferably used as the gate insulating film in order to form a favorable interface with the oxide semiconductor.
- an element with a channel width W of 1 ⁇ 10 4 ⁇ m and a channel length of 3 ⁇ m is highly expected to have the following characteristics of a thin film transistor: the off current is 10 ⁇ 13 A or less, and the subthreshold swing (S value) is 0.1 V/dec. (the thickness of the gate insulating film: 100 nm).
- FIG. 2 is a top view illustrating an example of a microwave plasma apparatus.
- a common chamber 1120 is connected to load/unload (L/UL) chambers 1110 and 1115 and reaction chambers ( 1 ) 1111 to ( 4 ) 1114 via gate valves 1122 to 1127 .
- a substrate 1130 is set in a cassette 1128 of the load/unload (L/UL) chamber 1110 or a cassette 1129 of the load/unload (L/UL) chamber 1115 and transferred to the reaction chambers by a transfer unit 1121 of the common chamber 1120 .
- the microwave plasma CVD apparatus is provided with a plurality of load/unload (L/UL) chambers but may be provided with only one load/unload (L/UL) chamber.
- the high-density plasma CVD apparatus may be provided with a pretreatment chamber. By pre-heating the substrate in the pretreatment chamber, heating time before deposition in each reaction chamber can be shortened; accordingly, the throughput can be improved.
- FIG. 3 illustrates a detailed structure of a reaction chamber of the microwave plasma CVD apparatus used for forming a gate insulating film.
- the reaction chamber of the microwave plasma CVD apparatus includes a treatment container 180 , a support 181 which is provided in the treatment container 180 and on which the substrate 1130 is set, an exhaust port 183 connected to a vacuum pump for exhausting a gas in the treatment container 180 , a microwave generation unit 184 for supplying microwaves for generating plasma, a waveguide 185 for introducing microwaves from a microwave supply unit to the treatment container 180 , a top plate 187 which is in contact with the waveguide 185 and has openings 187 a , and a plurality of dielectric plates 186 fixed to the top plate 187 with a fixing member 188 .
- the substrate 1130 is provided to face the dielectric plates 186 .
- the vacuum pump a dry pump for low vacuum evacuation and a turbo molecular pump for high vacuum evacuation can be used.
- a substrate having a size of 600 mm ⁇ 720 mm is used as the substrate 1130 . Note that there is no limitation on the size of the substrate.
- a gas pipe 197 through which a non-source gas flows and a gas pipe 198 through which a source gas flows are provided between the substrate 1130 and the dielectric plates 186 .
- the gas pipe 197 through which a non-source gas flows is connected to a non-source gas supply source 191 via a valve 195 and a mass flow controller 193 .
- the gas pipe 198 through which a source gas flows is connected to a source gas supply source 192 via a valve 196 and a mass flow controller 194 .
- a temperature control portion 199 for the support 181 By provision of a temperature control portion 199 for the support 181 , the temperature of the substrate 1130 can be controlled.
- a high-frequency power source may be connected to the support 181 , so that predetermined bias voltage is applied to the support 181 by AC electric power output from the high-frequency power source.
- the microwave generation unit 184 is preferably provided outside the treatment container 180 .
- the microwave generation unit 184 supplies microwaves.
- the plurality of microwave generation units 184 is provided, stable large-sized plasma can be generated. Therefore, a highly uniform film can be formed over a large-sized substrate with one side of over 600 mm, particularly over 1000 mm, and the deposition rate can be increased.
- the treatment container 180 and the top plate 187 are formed using metal whose surface is covered with an insulating film of alumina, silicon oxide, or a fluorine resin, for example, an alloy including aluminum. Further, the fixing member 188 is formed using metal such as an alloy including aluminum.
- the dielectric plates 186 are provided so as to be in close contact with the openings of the top plate 187 .
- the microwaves generated in the microwave generation unit 184 are propagated to the dielectric plates 186 by passing through the waveguide 185 and the openings 187 a of the top plate 187 and transmitted through the dielectric plates 186 to be released into the treatment container.
- the non-source gas is excited into a plasma state.
- This plasma 200 has higher density on the surface of the dielectric plates 186 ; thus, damage to the substrate 1130 can be reduced.
- the dielectric plates 186 are formed using ceramics such as sapphire, quartz glass, alumina, silicon oxide, or silicon nitride.
- the dielectric plates 186 may have a recessed portion 189 on the side where the plasma 200 is generated. With the recessed portion 189 , stable plasma can be generated. Furthermore, by provision of the plurality of dielectric plates 186 , a highly uniform film can be formed over a large-sized substrate with one side of over 600 mm, particularly over 1000 mm, and the deposition rate can be increased.
- the non-source gas flows through the plurality of gas pipes 197 on the upper side, and the source gas flows through the plurality of gas pipes 198 on the lower side.
- the gas pipes 197 and 198 are provided to intersect with each other. Outlets of the gas pipes 197 through which the non-source gas flows are provided on the dielectric plates 186 side, and outlets of the gas pipes 198 through which the source gas flows are provided on the substrate 1130 side.
- the plurality of gas pipes 197 and the plurality of gas pipes 198 are provided to intersect with each other, the distance between the gas pipes can be shortened and thus the distance between the outlets can be shortened; accordingly, deposition can be uniformly performed over the substrate 1130 . This structure is particularly effective when a large-sized substrate is used.
- the plasma 200 can be generated while a film is prevented from being formed on the surface of the dielectric plates 186 . Further, since the source gas is ejected toward the substrate 1130 , the source gas can be ejected from a position closer to the substrate 1130 , and thus the deposition rate can be increased. Note that part of the source gas can flow through the gas pipes 197 on the upper side.
- the gas pipes 197 and 198 are formed using ceramics such as alumina or aluminum nitride. Transmissivity of the microwaves is high in ceramics; therefore, when the gas pipes 197 and 198 are formed using ceramics, distribution of the plasma can be uniform without an electric field being disturbed, even when the gas pipes are provided right under the dielectric plates 186 .
- Deposition treatment of the gate insulating film 102 is described below.
- the deposition treatment starts at a step S 170 in FIG. 4 .
- the temperature of the substrate 1130 is controlled at a step S 171 .
- the substrate 1130 is at room temperature or heated to 100° C. to 550° C. by the temperature control portion 199 .
- the inside of the treatment container 180 is made into a vacuum state, and one or more rare gases such as helium, argon, xenon, and krypton are introduced into the treatment container 180 as a gas for generating plasma.
- one or more rare gases such as helium, argon, xenon, and krypton are introduced into the treatment container 180 as a gas for generating plasma.
- oxygen is introduced into the treatment container 180 together with the rare gas, plasma can be easily generated.
- the distance between the substrate 1130 and the dielectric plates 186 is approximately 10 mm to 200 mm (preferably 110 mm to 160 mm).
- the pressure in the treatment container 180 is set at predetermined pressure, 1 Pa to 200 Pa, preferably 1 Pa to 100 Pa, more preferably 1 Pa to 40 Pa.
- the microwave generation unit 184 is turned on, and microwaves are supplied from the microwave generation unit 184 to the waveguide 185 , so that plasma is generated in the treatment container 180 .
- the output power of the microwave generation unit is set at 500 W to 6000 W, preferably 4000 W to 6000 W.
- plasma with low electron temperature higher than or equal to 0.7 eV and lower than or equal to 3 eV, preferably higher than or equal to 0.7 eV and lower than or equal to 1.5 eV
- high electron density (1 ⁇ 10 11 atoms/cm 3 to 1 ⁇ 10 13 atoms/cm 3
- a source gas is introduced from the gas pipes 198 into the treatment container 180 . Specifically, supply of oxygen is halted, and dinitrogen monoxide, a rare gas, and silicon hydride or silicon halide are introduced as a source gas, whereby a silicon oxynitride film can be formed over the substrate 1130 .
- step S 176 supply of the source gas is halted, the pressure in the treatment container is lowered, and the microwave generation unit is turned off, so that the deposition process finishes at a step S 177 .
- a silicon oxynitride film which withstands high voltage can be formed under the following conditions: the substrate temperature is 300° C. to 350° C.; and the flow rate of dinitrogen monoxide is greater than or equal to 10 times and less than or equal to 300 times, preferably greater than or equal to 50 times and less than or equal to 200 times, of that of silicon hydride or silicon halide.
- the withstand voltage of the silicon oxynitride film can be increased under the following conditions: 2 to 6 microwave generation units with power of 5 kW are used; the pressure in the treatment container is 10 Pa to 100 Pa, preferably 10 Pa to 50 Pa; and the distance between the substrate 1130 and the dielectric plates 186 is greater than or equal to 110 mm and less than or equal to 160 mm.
- FIG. 16 is a plain view illustrating an example of a structure of the waveguide 185 .
- the waveguide 185 extends in parallel with the top plate 187 , and the plurality of waveguides 185 is provided in parallel with each other.
- the dielectric plates 186 are provided on the top plate 187 in a matrix form.
- the waveguides 185 and the openings 187 a formed in the top plate 187 are provided to be aligned with the dielectric plates 186 .
- the waveguide 185 is preferably divided into plural parts and microwaves are supplied.
- FIG. 16 illustrates a structure in which branch waveguides are used at an end portion of each waveguide 185 , and the microwaves divided into a plurality are supplied.
- a microwave power supply is connected to the tip of each branch waveguide. Use of a plurality of microwave power supplies makes it possible to keep uniformity of plasma even when the area of the substrate to be processed becomes large.
- a silicon oxynitride film is formed as the gate insulating film in this embodiment, a silicon nitride film can also be formed. In that case, silane and nitrogen can be used as a source gas.
- FIG. 10A shows the characteristics of a thin film transistor whose gate insulating film is formed with the microwave plasma CVD apparatus described in this embodiment
- FIG. 10B shows the characteristics of a thin film transistor whose gate insulating film is formed with a conventional plasma CVD apparatus. The results are compared with each other.
- the gate BT test is a test for evaluating the reliability of a transistor from the amount of shift in threshold voltage (Vth) or the like. The smaller the shift amount is, the more stable the operation of a transistor is and the higher the reliability thereof is.
- threshold voltage (Vth) the thin film transistor formed by the conventional method ( FIG. 10B ) is normally on and variation in a substrate surface is ⁇ 4.2 V, while the thin film transistor of this embodiment ( FIG. 10A ) is normally off and variation in a substrate surface is largely reduced to ⁇ 1.0 V.
- a gate insulating film As described above, by forming a gate insulating film with use of a microwave plasma CVD apparatus, dangling bonds in the gate insulating film are reduced and the interface between the gate insulating film and an oxide semiconductor can be favorable. Accordingly, the characteristics of a manufactured thin film transistor can be improved.
- the source gas ejected from the gas pipes 198 on the lower side is blown up by the non-source gas ejected from the gas pipes 197 on the upper side as illustrated in FIG. 3 .
- the blown source gas is deposited on the dielectric plates 186 or the like as powder or a film.
- the deposited powder or film might fall onto the substrate 1130 over time and cause a particle.
- a structure with which particles are reduced is described.
- a reaction chamber illustrated in FIG. 5 includes, instead of the gas pipes 197 on the upper side in FIG. 3 , a plurality of members 300 (also referred to as beams) provided in parallel with the dielectric plates 186 . Gas outlets of the members 300 are provided on the substrate 1130 side and eject a non-source gas. In addition, gas outlets of the gas pipes 198 provided between the substrate 1130 and the dielectric plates 186 are provided on the substrate 1130 side and eject a source gas. That is, both the gas pipes 198 and the members 300 eject the gasses to the substrate 1130 side.
- outlets of the members 300 are connected to the non-source gas supply source 191 via a gas pipe inside the apparatus, the valve 195 , and the mass flow controller 193 . Further, the gas pipes 198 through which the source gas flows are connected to the source gas supply source 192 via the valve 196 and the mass flow controller 194 . Note that a structure in which part of the source gas is ejected from the members 300 can also be employed.
- the gas pipes 198 are preferably provided to intersect with the members 300 having the outlets. As illustrated in FIG. 5 , when the plurality of gas pipes 198 and the plurality of members 300 are provided to intersect with each other, the distance between the members 300 and the distance between the gas pipes 198 can be shortened and thus the distance between the outlets can be shortened; accordingly, deposition can be uniformly performed over the substrate 1130 . This structure is particularly effective when a large-sized substrate is used. It is also effective that the outlets of the members 300 do not overlap with the gas pipes 198 . If they overlap with each other, the gas ejected from the members 300 might be blown up.
- the source gas can be prevented from being blown up and generation of particles can be suppressed.
- the structure of this embodiment is particularly effective when the flow rate ratio of dinitrogen monoxide to silane is high, because particles are easily generated under such a condition.
- the thin film transistor is manufactured by sequentially forming the gate electrode 101 , the gate insulating film 102 , the oxide semiconductor film 108 , the source electrode 106 and the drain electrode 107 , the insulating film 109 , a back-gate electrode 601 , and an insulating film 602 over the substrate 100 with an insulating property.
- the microwave plasma CVD apparatus described in Embodiment 2 or 3 can be used. Dangling bonds in the gate insulating film 102 can be reduced and the interface between the oxide semiconductor film 108 and the gate insulating film 102 can be favorable.
- the back-gate electrode 601 is formed in a position overlapping with the oxide semiconductor film 108 in such a manner that a conductive film is formed over the insulating film 109 and then the conductive film is patterned.
- the back-gate electrode 601 can be formed using a material and a structure similar to those of the gate electrode 101 , or the source electrode 106 and the drain electrode 107 .
- the thickness of the back-gate electrode 601 is 10 nm to 400 nm, preferably 100 nm to 200 nm.
- a conductive film having a structure in which a titanium film, an aluminum film, and a titanium film are stacked is formed.
- a resist mask is formed by a photolithography method, and an unnecessary portion is removed by etching so that the conductive film is processed (patterned) into a desired shape; thus, the back-gate electrode 601 is formed.
- the insulating film 602 is preferably formed using a material with a high barrier property that can prevent moisture, hydrogen, oxygen, and the like in an atmosphere from affecting the characteristics of the transistor.
- the insulating film can be formed to have a single-layer structure or a stacked-layer structure using an insulating film with a high barrier property such as a silicon nitride film, a silicon nitride oxide film, an aluminum nitride film, or an aluminum nitride oxide film by a plasma CVD method, a sputtering method, or the like.
- the insulating film 602 is preferably formed to a thickness of 15 nm to 400 nm, for example.
- the back-gate electrode 601 may be electrically insulated and in a floating state, or may be supplied with a potential. In the latter case, the back-gate electrode 601 may be supplied with the same potential as the gate electrode 101 , or may be supplied with a fixed potential such as a ground potential. By controlling the level of a potential supplied to the back-gate electrode 601 , the threshold voltage of the transistor is controlled; consequently, variation in the threshold voltage in a substrate surface can be reduced.
- FIGS. 11A and 11B the characteristics of a thin film transistor provided with a back-gate electrode and those of a thin film transistor without a back-gate electrode are compared.
- FIG. 11A shows the results in the case of forming a back-gate electrode as in this embodiment.
- FIG. 11B shows the results in the case of not forming a back-gate electrode as in Embodiment 1 (which is the same as FIG. 10A ).
- a bottom-gate thin film transistor having a channel protective structure will be described with reference to FIG. 7 .
- FIG. 7 illustrates an example of a cross-sectional structure of a bottom-gate thin film transistor having a channel protective structure.
- the thin film transistor is manufactured by sequentially forming the gate electrode 101 , the gate insulating film 102 , the oxide semiconductor film 104 , a channel protective film 701 , the source electrode 106 and the drain electrode 107 , and the insulating film 109 over the substrate 100 with an insulating property.
- the channel protective film 701 is formed over the oxide semiconductor film 104 so as to overlap with a channel formation region of the oxide semiconductor film 104 .
- the channel protective film 701 can prevent the portion of the oxide semiconductor film 104 , which serves as the channel formation region, from being damaged in a later step (e.g., reduction in thickness due to plasma or an etchant in etching). Therefore, the reliability of the thin film transistor can be improved.
- the channel protective film 701 can be formed using an inorganic material including oxygen (such as silicon oxide, silicon oxynitride, or silicon nitride oxide).
- oxygen such as silicon oxide, silicon oxynitride, or silicon nitride oxide.
- the microwave plasma CVD apparatus described in Embodiment 2 or 3 can be used. Dangling bonds in the gate insulating film 102 can be reduced and the interface between the oxide semiconductor film 104 and the gate insulating film 102 can be favorable.
- a top-gate thin film transistor will be described with reference FIG. 8 .
- FIG. 8 illustrates an example of a cross-sectional structure of a top-gate thin film transistor.
- the thin film transistor is manufactured by sequentially forming an insulating film 801 , an oxide semiconductor film 802 , a source electrode 803 and a drain electrode 804 , a gate insulating film 805 , and a gate electrode 806 over a substrate 800 having an insulating surface.
- the microwave plasma CVD apparatus described in Embodiment 2 or 3 can be used. Dangling bonds in the gate insulating film 805 can be reduced and the interface between the oxide semiconductor film 802 and the gate insulating film 805 can be favorable.
- the microwaves By using the microwaves with a frequency of 1 GHz or lower, the uniformity of plasma in a reaction chamber can be maintained even when the kind of gasses is changed or the pressure is changed in a wide range.
- the frequency is preferably 915 MHz.
- a gate insulating film having a structure different from that of other embodiments will be described. Any of the structures and manufacturing methods of other embodiments other than the gate insulating film can be applied to this embodiment.
- the gate insulating film has a stacked-layer structure of a first insulating film formed by microwave plasma CVD and a second insulating film with a higher dielectric constant than the first insulating film.
- the first insulating film formed by microwave plasma CVD is used as an insulating film that is in contact with an oxide semiconductor film, whereby the quality of the interface therebetween is improved.
- a thick insulating film with a higher dielectric constant than the first insulating film is used as the second insulating film that is not in contact with the oxide semiconductor, whereby the channel capacitance can be secured with leakage current suppressed.
- an oxide film, a nitride film, an oxynitride film, a nitride oxide film, or the like including hafnium (Hf), zirconium (Zr), lanthanum (La), or the like can be used.
- a film of hafnium oxide or the like may be formed by a sputtering method. Even when the second insulating film is formed by a sputtering method, the first insulating film is provided between the second insulating film and the oxide semiconductor; therefore, the quality of the interface with the oxide semiconductor is improved.
- the gate insulating film of this embodiment may be applied to a bottom-gate transistor like that in FIGS. 1A to 1E , FIG. 6 , or FIG. 7 or may be applied to a top-gate transistor like that in FIG. 8 .
- FIG. 9A illustrates an example of electronic paper (also referred to as an electronic book reader).
- FIG. 9B illustrates an example of a display device.
- FIG. 9C illustrates an example of a display device having flexibility.
- FIG. 9D illustrates an example of a portable game machine.
- FIG. 9E illustrates an example of a mobile phone.
- a semiconductor device according to an embodiment of the present invention can be used for display portions 7011 to 7015 provided for main bodies 7001 to 7005 . Note that the semiconductor device according to an embodiment of the present invention can also be used for an electronic device which does not have a display portion.
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Abstract
It is an object to drive a semiconductor device at high speed or to improve the reliability of the semiconductor device. In a method for manufacturing the semiconductor device, in which a gate electrode is formed over a substrate with an insulating property, a gate insulating film is formed over the gate electrode, and an oxide semiconductor film is formed over the gate insulating film, the gate insulating film is formed by deposition treatment using high-density plasma. Accordingly, dangling bonds in the gate insulating film are reduced and the quality of the interface between the gate insulating film and the oxide semiconductor is improved.
Description
- The present invention relates to a semiconductor device and a method for manufacturing the semiconductor device. The present invention particularly relates to a semiconductor device including an oxide semiconductor and a method for manufacturing the semiconductor device. Further, the present invention relates to an apparatus used for manufacturing a semiconductor device.
- A thin film transistor including a semiconductor film formed over an insulating surface is an essential semiconductor element for a semiconductor device. Since there is limitation on the allowable temperature limit of a substrate in manufacture of a thin film transistor, a thin film transistor in which amorphous silicon that can be deposited at a relatively low temperature, polysilicon that can be obtained by crystallization with use of laser light or a catalytic element, or the like is included in an active layer is mainly used for a semiconductor display device.
- In recent years, a metal oxide having semiconductor characteristics which is referred to as an oxide semiconductor has attracted attention as a novel semiconductor material which has both high electron mobility, which is a characteristic of polysilicon, and uniform element characteristics, which is a characteristic of amorphous silicon. The metal oxide is used for various applications. For example, indium oxide is a well-known metal oxide and used as a material of a transparent electrode included in a liquid crystal display device or the like. Examples of such metal oxides having semiconductor characteristics include tungsten oxide, tin oxide, indium oxide, and zinc oxide. Thin film transistors in which a channel formation region is formed using such a metal oxide having semiconductor characteristics are known (Patent Documents 1 and 2).
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- [Patent Document 1] Japanese Published Patent Application No. 2007-123861
- [Patent Document 2] Japanese Published Patent Application No. 2007-96055
- A transistor used for a semiconductor device is required to have favorable transistor characteristics such as on current, off current, and electron mobility. By using a transistor having favorable characteristics, the semiconductor device can be driven at higher speed. In addition, by preventing deterioration or variation of a transistor to improve the reliability, a highly reliable semiconductor device can be provided.
- Thus, it is an object to provide a semiconductor device which can be driven at high speed and a method for manufacturing the semiconductor device. It is another object to provide a highly reliable semiconductor device and a method for manufacturing the semiconductor device.
- It is another object to provide a novel CVD apparatus.
- According to an embodiment of the present invention, the purity of an oxide semiconductor used in a channel formation region of a transistor is increased and the quality of a gate insulating film which is in contact with the oxide semiconductor is improved. In other words, an i-type or substantially i-type oxide semiconductor (a highly purified oxide semiconductor) which is obtained by removal of an impurity is extremely sensitive to an interface state or an interface charge; therefore, the conditions of a gate insulating film and the interface between the gate insulating film and an oxide semiconductor film need to be kept favorable.
- In order to increase the purity of the oxide semiconductor, it is necessary to remove, from the oxide semiconductor, hydrogen that serves as a donor in the oxide semiconductor and becomes a factor causing the oxide semiconductor to be an n-type oxide semiconductor. Then, oxygen is supplied to a deficient portion from which hydrogen is removed and oxygen is supplied to compensate oxygen which is lost at the same time as the removal of hydrogen, whereby the oxide semiconductor film is highly purified.
- Further, a dense insulating film having few defects is used as the gate insulating film which is in contact with the highly purified oxide semiconductor film.
- The defect here refers to a dangling bond or the like in the gate insulating film. By reducing the dangling bond or the like, the characteristics of the interface between the oxide semiconductor and the gate insulating film becomes favorable and the transistor characteristics are improved.
- Therefore, in accordance with the present invention, as a method for reducing dangling bonds in the gate insulating film, formation of a gate insulating film by deposition treatment using high-density plasma is provided.
- By using high-density plasma, plasma damage to the gate insulating film is reduced and thus a gate insulating film in which defects are largely reduced is formed.
- An embodiment of the present invention is a method for manufacturing a semiconductor device which includes a gate electrode, an oxide semiconductor film, and a gate insulating film that is formed using a high-density plasma CVD apparatus, including the steps of: setting a substrate to face a dielectric plate provided in a reaction chamber of the high-density plasma CVD apparatus; ejecting a gas for generating plasma toward the dielectric plate to generate plasma; and ejecting a source gas of the gate insulating film toward the substrate, so that the gate insulating film is formed.
- Another embodiment of the present invention is a method for manufacturing a semiconductor device which includes a gate electrode, an oxide semiconductor film, and a gate insulating film that is formed using a high-density plasma CVD apparatus, including the steps of: setting a substrate to face a dielectric plate provided in a reaction chamber of the high-density plasma CVD apparatus; ejecting a gas for generating plasma toward the dielectric plate from a first gas pipe to generate plasma; and ejecting a source gas of the gate insulating film toward the substrate from a second gas pipe which is provided to intersect with the first gas pipe, so that the gate insulating film is formed.
- Another embodiment of the present invention is a method for manufacturing a semiconductor device which includes a gate electrode, an oxide semiconductor film, and a gate insulating film that is formed using a high-density plasma CVD apparatus, including the steps of: setting a substrate to face a dielectric plate provided in a reaction chamber of the high-density plasma CVD apparatus; ejecting a gas for generating plasma toward the substrate to generate plasma; and ejecting a source gas of the gate insulating film toward the substrate, so that the gate insulating film is formed.
- Another embodiment of the present invention is a method for manufacturing a semiconductor device which includes a gate electrode, an oxide semiconductor film, and a gate insulating film that is formed using a high-density plasma CVD apparatus, including the steps of: setting a substrate to face a dielectric plate provided in a reaction chamber of the high-density plasma CVD apparatus; ejecting a gas for generating plasma toward the substrate from a member provided in parallel with the dielectric plate to generate plasma; and ejecting a source gas of the gate insulating film toward the substrate from a gas pipe which is provided to intersect with the member, so that the gate insulating film is formed.
- By forming a gate insulating film with use of a high-density plasma CVD apparatus, the characteristics of the interface between an oxide semiconductor film and the gate insulating film can be improved.
- By improving the interface characteristics, the transistor characteristics such as on current, off current, electron mobility, and reliability become favorable; accordingly, a semiconductor device can operate at high speed and the reliability thereof can be improved.
- In the accompanying drawings:
-
FIGS. 1A to 1E are cross-sectional views of a semiconductor device; -
FIG. 2 is a top view of a manufacturing apparatus; -
FIG. 3 is a cross-sectional view of a manufacturing apparatus; -
FIG. 4 is a flow chart; -
FIG. 5 is a cross-sectional view of a manufacturing apparatus; -
FIG. 6 is a cross-sectional view of a semiconductor device; -
FIG. 7 is a cross-sectional view of a semiconductor device; -
FIG. 8 is a cross-sectional view of a semiconductor device; -
FIGS. 9A to 9E illustrate examples of electronic devices; -
FIGS. 10A and 10B show characteristics of transistors; -
FIGS. 11A and 11B show characteristics of transistors; -
FIG. 12 is a longitudinal sectional view of a bottom-gate thin film transistor including an oxide semiconductor; -
FIGS. 13A and 13B are energy band diagrams (schematic diagrams) along a section A-A′ inFIG. 12 ; -
FIG. 14A illustrates the state where a positive potential (+VG) is applied to a gate (G1), and 14B illustrates the state where a negative potential (−VG) is applied to the gate (G1); -
FIG. 15 illustrates relations between the vacuum level and the work function of a metal (φM) and between the vacuum level and the electron affinity (χ) of an oxide semiconductor; and -
FIG. 16 is a plan view of a manufacturing apparatus. - Embodiments of the present invention will be described below with reference to the drawings. Note that the present invention can be implemented in many different modes, and it is easily understood by those skilled in the art that modes and details of the present invention can be modified in various ways without departing from the sprit and the scope of the present invention. Therefore, the present invention is not construed as being limited to description of the embodiments.
- A method for manufacturing a semiconductor device will be described with reference to
FIGS. 1A to 1E by taking a bottom-gate thin film transistor having a channel-etched structure as an example. - As illustrated in
FIG. 1A , agate electrode 101 is formed over asubstrate 100. As thesubstrate 100, the following can be used: an alkali-free glass substrate manufactured by a fusion method or a floating method, such as a barium borosilicate glass substrate, an aluminoborosilicate glass substrate, or an aluminosilicate glass substrate; a ceramic substrate; a plastic substrate with heat resistance enough to withstand a process temperature in this manufacturing process; or the like. Alternatively, a metal substrate such as a stainless steel alloy substrate having a surface provided with an insulating layer may be used. As thesubstrate 100, a substrate having a size of 320 mm×400 mm, 370 mm×470 mm, 550 mm×650 mm, 600 mm×720 mm, 680 mm×880 mm, 730 mm×920 mm, 1000 mm×1200 mm, 1100 mm×1250 mm, 1150 mm×1300 mm, 1500 mm×1800 mm, 1900 mm×2200 mm, 2160 mm×2460 mm, 2400 mm×2800 mm, 2850 mm×3050 mm, or the like can be used. - An insulating film serving as a base film may be formed between the
substrate 100 and thegate electrode 101. As the base film, for example, a single layer of a silicon oxide film, a silicon oxynitride film, a silicon nitride film, a silicon nitride oxide film, an aluminum nitride film, or an aluminum nitride oxide film or a stacked layer of a plurality of these films can be used. In particular, when an insulating film with a high barrier property, such as a silicon nitride film, a silicon nitride oxide film, an aluminum nitride film, or an aluminum nitride oxide film is used as the base film, impurities in an atmosphere such as moisture or hydrogen, or impurities included in thesubstrate 100 such as alkali metal or heavy metal can be prevented from entering an oxide semiconductor film, a gate insulating film, an interface between the oxide semiconductor film and the gate insulating film or the like, or the vicinity of the interface. - In this specification, oxynitride refers to a substance which includes more oxygen than nitrogen, and nitride oxide refers to a substance which includes more nitrogen than oxygen. For example, silicon oxynitride is a substance including oxygen, nitrogen, silicon, and hydrogen in the ranges of greater than or equal to 50 atomic % and less than or equal to 70 atomic %, greater than or equal to 0.5 atomic % and less than or equal to 15 atomic %, greater than or equal to 25 atomic % and less than or equal to 35 atomic %, and greater than or equal to 0.1 atomic % and less than or equal to 10 atomic %, respectively. Further, silicon nitride oxide is a substance including oxygen, nitrogen, silicon, and hydrogen in the ranges of greater than or equal to 5 atomic % and less than or equal to 30 atomic %, greater than or equal to 20 atomic % and less than or equal to 55 atomic %, greater than or equal to 25 atomic % and less than or equal to 35 atomic %, and greater than or equal to 10 atomic % and less than or equal to 30 atomic %, respectively. Note that the above ranges are obtained by measurement using Rutherford backscattering spectrometry (RBS) or hydrogen forward scattering spectrometry (HFS). In addition, the total of the percentages of the constituent elements does not exceed 100 atomic %.
- The
gate electrode 101 can be formed using a single layer or a stacked layer of one or more conductive films including a metal material such as molybdenum, titanium, chromium, tantalum, tungsten, neodymium, or scandium, or an alloy material which includes any of these metal materials as a main component; or a nitride of any of these metals. Note that aluminum or copper can also be used as the above metal material as long as it can withstand the temperature of heat treatment performed in a later step. Aluminum or copper is preferably used in combination with a refractory metal material in order to avoid problems of heat resistance and corrosion. As the refractory metal material, molybdenum, titanium, chromium, tantalum, tungsten, neodymium, scandium, or the like can be used. - For example, as a two-layer structure of the
gate electrode 101, the following structures are preferable: a two-layer structure in which a molybdenum film is stacked over an aluminum film; a two-layer structure in which a molybdenum film is stacked over a copper film; a two-layer structure in which a titanium nitride film or a tantalum nitride film is stacked over a copper film; and a two-layer structure in which a titanium nitride film and a molybdenum film are stacked. As a three-layer structure of thegate electrode 101, the following structure is preferable: a stacked-layer structure including an aluminum film, an alloy film of aluminum and silicon, an alloy film of aluminum and titanium, or an alloy film of aluminum and neodymium in a middle layer and any of a tungsten film, a tungsten nitride film, a titanium nitride film, and a titanium film in a top layer and a bottom layer. - Further, when a light-transmitting oxide conductive film of indium oxide, an alloy of indium oxide and tin oxide, an alloy of indium oxide and zinc oxide, zinc oxide, zinc aluminum oxide, zinc aluminum oxynitride, zinc gallium oxide, or the like is used for the
gate electrode 101, the aperture ratio of a pixel portion can be improved. - The
gate electrode 101 is formed to a thickness of 10 nm to 400 nm, preferably 100 nm to 200 nm In this embodiment, a conductive film for the gate electrode is formed to a thickness of 150 nm by a sputtering method using a tungsten target, and then the conductive film is processed (patterned) into a desired shape by etching; thus, thegate electrode 101 is formed. - Next, a
gate insulating film 102 is formed over thegate electrode 101. - The
gate insulating film 102 is preferably formed by deposition treatment using high-density plasma. With high-density plasma, plasma damage to thegate insulating film 102 can be reduced. Accordingly, dangling bonds in thegate insulating film 102 can be reduced and defects can be reduced; thus, the interface with an oxide semiconductor formed later can be highly favorable. - The
gate insulating film 102 can be formed to have a single-layer or stacked-layer structure with use of any of materials such as a silicon oxide film, a silicon nitride film, a silicon oxynitride film, and a silicon nitride oxide film. For example, a silicon oxynitride film is formed using silane and nitrogen monoxide as a deposition gas. The thickness of thegate insulating film 102 is greater than or equal to 100 nm and less than or equal to 500 nm In the case of a stacked-layer structure, for example, a first gate insulating film with a thickness of greater than or equal to 50 nm and less than or equal to 200 nm and a second gate insulating film with a thickness of greater than or equal to 5 nm and less than or equal to 300 nm are stacked in this order. - Further, the
gate insulating film 102 can be formed by stacking a silicon oxide film or a silicon oxynitride film, and a silicon nitride film or a silicon nitride oxide film in this order from the substrate side. Alternatively, thegate insulating film 102 can be formed by stacking a silicon nitride film or a silicon nitride oxide film, a silicon oxide film or a silicon oxynitride film, and a silicon nitride film or a silicon nitride oxide film in this order from the substrate side. - In this embodiment, as the
gate insulating film 102, a 100-nm-thick silicon oxynitride film is formed by plasma CVD using microwaves of 2.45 GHz as high-density plasma. In this specification, a microwave refers to a wave in the frequency range of 300 MHz to 300 GHz. - Note that before an oxide semiconductor film is formed by a sputtering method, dust attached to a surface of the
gate insulating film 102 is preferably removed by reverse sputtering in which an argon gas is introduced and plasma is generated. The reverse sputtering refers to a method in which, without application of voltage to a target side, an RF power source is used for application of voltage to a substrate side in an argon atmosphere so that plasma is generated in the vicinity of the substrate to modify a surface. Note that instead of an argon atmosphere, a nitrogen atmosphere, a helium atmosphere, or the like may be used. Alternatively, an argon atmosphere to which oxygen, nitrous oxide, or the like is added may be used. Further alternatively, an argon atmosphere to which chlorine, carbon tetrafluoride, or the like is added may be used. - As the oxide semiconductor film, an oxide semiconductor film such as an In—Sn—Ga—Zn—O film, an In—Ga—Zn—O film, an In—Sn—Zn—O film, an In—Al—Zn—O film, a Sn—Ga—Zn—O film, an Al—Ga—Zn—O film, a Sn—Al—Zn—O film, an In—Zn—O film, a Sn—Zn—O film, an Al—Zn—O film, a Zn—Mg—O film, a Sn—Mg—O film, an In—Mg—O film, an In—O film, a Sn—O film, or a Zn—O film can be used. Further, the oxide semiconductor film may include SiO2.
- As the oxide semiconductor film, a thin film expressed by InMO3(ZnO)m (m>0) can be used. Here, M represents one or more metal elements selected from Ga, Al, Mn, and Co. For example, M is Ga, Ga and Al, Ga and Mn, Ga and Co, or the like. An oxide semiconductor film whose composition formula is expressed by InMO3 (ZnO)m (m>0) where Ga is included as M is referred to as an In—Ga—Zn—O oxide semiconductor, and a thin film of the In—Ga—Zn—O oxide semiconductor is also referred to as an In—Ga—Zn—O-based non-single-crystal film.
- The thickness of the oxide semiconductor film is 10 nm to 300 nm, preferably 20 nm to 100 nm. In this embodiment, as the oxide semiconductor film, a 30-nm-thick In—Ga—Zn—O-based non-single-crystal film which is obtained by a sputtering method using a metal oxide target including indium (In), gallium (Ga), and zinc (Zn) (In2O3:Ga2O3:ZnO=1:1:1 or In2O3:Ga2O3:ZnO=1:1:2 in a molar ratio) is used. In this embodiment, a DC sputtering method is used, the flow rate of argon is 30 sccm, the flow rate of oxygen is 15 sccm, and the substrate temperature is room temperature.
- Next, as illustrated in
FIG. 1A , the oxide semiconductor film is processed (patterned) into a desired shape by etching or the like, so that an island-shapedoxide semiconductor film 103 is formed over thegate insulating film 102 to overlap with thegate electrode 101. - Next, the
oxide semiconductor film 103 may be subjected to heat treatment in an atmosphere of an inert gas (such as nitrogen, helium, neon, or argon). When the heat treatment is performed on theoxide semiconductor film 103, anoxide semiconductor film 104 from which moisture and hydrogen are eliminated is formed. Specifically, rapid thermal annealing (RTA) treatment can be performed in an atmosphere of an inert gas (such as nitrogen, helium, neon, or argon) at a temperature of higher than or equal to 500° C. and lower than or equal to 750° C. (or a temperature lower than or equal to the strain point of the glass substrate) for approximately 1 minute to 10 minutes, preferably at 600° C. for approximately 3 minutes to 6 minutes. With an RTA method, dehydration or dehydrogenation can be performed in a short time; therefore, treatment can be performed even at a temperature higher than the strain point of the glass substrate. Note that the timing of the above heat treatment is not limited to after formation of the island-shapedoxide semiconductor film 103, and the oxide semiconductor film before being processed into the island-shapedoxide semiconductor film 103 may be subjected to the heat treatment. The heat treatment may also be performed plural times after the formation of theoxide semiconductor film 104. - In the island-shaped
oxide semiconductor film 104, hydrogen included in the oxide semiconductor is reduced by the above heat treatment, and oxygen is introduced into a deficient portion from which hydrogen is removed and an oxygen-deficient portion, whereby the carrier concentration can be reduced, preferably to lower than 1×1014/cm3. By reducing impurities such as hydrogen which serves as a donor as much as possible in an oxide semiconductor with an energy gap of 2 eV or more, preferably 2.5 eV or more, more preferably 3 eV or more, the intrinsic carrier concentration thereof can be reduced to lower than or equal to 1.45×1010/cm3, which is that of silicon, and to approximately 10 −7/cm3 according to the Fermi-Dirac distribution law. - In this embodiment, heat treatment is performed for 6 minutes in a nitrogen atmosphere in the state where the substrate temperature reaches 600° C. For the heat treatment, a heating method using an electric furnace, a rapid heating method such as a gas rapid thermal annealing (GRTA) method using a heated gas or a lamp rapid thermal annealing (LRTA) method using lamp light, or the like can be used. For example, in the case of performing heat treatment using an electric furnace, the temperature rise characteristics are preferably set at higher than or equal to 0.1° C./min and lower than or equal to 20° C./min and the temperature drop characteristics are preferably set at higher than or equal to 0.1° C./min and lower than or equal to 15° C./min.
- Note that in the heat treatment, it is preferable that moisture, hydrogen, and the like be not included in nitrogen or a rare gas such as helium, neon, or argon. It is preferable that the purity of nitrogen or a rare gas such as helium, neon, or argon which is introduced into a heat treatment apparatus be 6N (99.9999%) or higher, preferably 7N (99.99999%) or higher (that is, the impurity concentration is 1 ppm or lower, preferably 0.1 ppm or lower).
- Alternatively, the heat treatment may be performed in air where the dew point under atmospheric pressure is −60° C. or lower and the moisture content is low, instead of an inert gas atmosphere such as a nitrogen atmosphere or a rare gas atmosphere.
- The island-shaped
oxide semiconductor film 104 which has been subjected to the heat treatment in an inert gas atmosphere is preferably in an amorphous state, but may be partly crystallized. - Next, as illustrated in
FIG. 1C , aconductive film 105 used for a source electrode and a drain electrode is formed over the island-shapedoxide semiconductor film 104. Theconductive film 105 is preferably formed using a material with low electronegativity, and may be formed using aluminum, magnesium, or the like by a sputtering method. Further, a film of titanium, tungsten, molybdenum, or the like which has low contact resistance with an oxide semiconductor may be formed between theoxide semiconductor film 104 and theconductive film 105 by a sputtering method. In order to prevent oxidation of theconductive film 105, a film of titanium, tungsten, molybdenum, or the like may be formed over theconductive film 105 by a sputtering method. A conductive film having a two-layer or three-layer structure is formed using any of these in combination as appropriate. - Note that the thickness of the
conductive film 105 may be 100 nm to 500 nm. - Next, as illustrated in
FIG. 1D , theconductive film 105 is processed (patterned) into a desired shape by etching or the like, so that asource electrode 106 and adrain electrode 107 are formed. - In the patterning for forming the
source electrode 106 and thedrain electrode 107, an exposed portion of the island-shapedoxide semiconductor film 104 is partly etched, so that an island-shapedoxide semiconductor film 108 having a groove (a recessed portion) is formed. - As illustrated in
FIG. 1E , after thesource electrode 106 and thedrain electrode 107 are formed, an insulatingfilm 109 is formed so as to cover thesource electrode 106, thedrain electrode 107, and theoxide semiconductor film 108. - As the insulating
film 109, a 200-nm-thick silicon oxide film is formed by a sputtering method. The insulatingfilm 109 can have a stacked-layer structure. - In this embodiment, impurities such as hydrogen included in the oxide semiconductor film are removed as much as possible to increase the purify of the oxide semiconductor film, and the interface characteristics with the gate insulating film which is in contact with the oxide semiconductor film are improved. Here, how such treatment affects the characteristics of a transistor is described below.
-
FIG. 12 is a cross-sectional view illustrating a thin film transistor manufactured in the above manner. An oxide semiconductor film (OS) is provided over a gate electrode (G1) with a gate insulating film (GI) interposed therebetween, and a source electrode (S) and a drain electrode (D) are provided over the oxide semiconductor film. Although a back-gate electrode (G2) is further provided inFIG. 12 , the back-gate electrode (G2) is not necessarily provided. -
FIGS. 13A and 13B are energy band diagrams (schematic diagrams) on A-A′ illustrated inFIG. 12 .FIG. 13A illustrates the case where the voltage between the source and the drain is 0 V (VD=0), andFIG. 13B illustrates the case where a positive potential with respect to the source is applied to the drain (VD>0). Note thatFIG. 13B illustrates the case where voltage is not applied to the gate (VG=0) (shown by a dashed line) and the case where positive voltage (VG>0) is applied to the gate (shown by a solid line). In the case where voltage is not applied to the gate, a carrier (electron) is not injected to the oxide semiconductor side from an electrode because of a high potential barrier, so that current does not flow, which means an off state. On the other hand, when positive voltage is applied to the gate, the potential barrier is lowered and thus current flows, which means an on state. -
FIGS. 14A and 14B are energy band diagrams (schematic diagrams) on B-B′ illustrated inFIG. 12 .FIG. 14A illustrates an on state in which a positive potential (+VG) is applied to the gate (G1) and carriers (electrons) flow between the source and the drain.FIG. 14B illustrates an off state in which a negative potential (−VG) is applied to the gate (G1) and minority carriers do not flow. -
FIG. 15 shows relations between the vacuum level and the work function of a metal (φM) and between the vacuum level and the electron affinity (χ) of an oxide semiconductor. - Electrons in metal degenerate at normal temperature, and its Fermi level is in a conduction band. On the other hand, a conventional oxide semiconductor is typically an n-type semiconductor, in which case the Fermi level (EF) is away from the intrinsic Fermi level (Ei) located in the middle of a band gap and is located closer to the conduction band. Note that it is known that part of hydrogen is a donor in an oxide semiconductor and is one factor causing an oxide semiconductor to be an n-type semiconductor.
- On the other hand, an oxide semiconductor of the present invention is an intrinsic (i-type) or a substantially intrinsic oxide semiconductor which is obtained by removing hydrogen that is an n-type impurity from an oxide semiconductor and purifying the oxide semiconductor so that the oxide semiconductor does not include an impurity other than a main component thereof as much as possible. In other words, a feature is that a purified i-type (intrinsic) semiconductor or a semiconductor close thereto is obtained not by adding an impurity but by removing an impurity such as hydrogen or water as much as possible. This enables the Fermi level (EF) to be at the same level as the intrinsic Fermi level (Ei).
- As one mode with which hydrogen is removed from the oxide semiconductor film (OS), metal with lower electronegativity than hydrogen may be used for a conductive film for the source electrode (S) and the drain electrode (D). By removing hydrogen that is an n-type impurity from the oxide semiconductor so that the oxide semiconductor does not include an impurity other than a main component thereof as much as possible, the oxide semiconductor can be highly purified.
- As another mode, the oxygen concentration of the oxide semiconductor film (OS) may be increased. By increasing the concentration of oxygen that is a main component of the oxide semiconductor, hydrogen that is an impurity can be removed and the oxide semiconductor can be highly purified. Heat treatment for removing hydrogen from the oxide semiconductor film (OS) is also effective.
- As another mode, an oxide film with high oxygen concentration may be formed as an insulating
film 1200 over the oxide semiconductor film (OS). Oxygen is supplied from the insulatingfilm 1200, whereby the oxygen concentration of the oxide semiconductor film (OS) can be increased. In addition, an effect of extraction of hydrogen in the oxide semiconductor film (OS) by oxygen in the insulatingfilm 1200 is obtained. The oxygen concentration of the insulatingfilm 1200 is set higher than the oxygen concentration of the oxide semiconductor film (OS). Further, in the case where the gate insulating film (GI) includes oxygen, hydrogen can also be efficiently extracted by the insulatingfilm 1200 by setting the oxygen concentration of the insulatingfilm 1200 higher than the oxygen concentration of the gate insulating film (GI). Note that the insulatingfilm 1200 is preferably formed by a sputtering method. - These modes may be combined as appropriate. In this manner, by removing hydrogen from the oxide semiconductor as much as possible, the oxide semiconductor can be highly purified. The hydrogen concentration may be reduced to, when measured by SIMS measurement, 5×1019/cm3 or lower, preferably 5×1018/cm3 or lower, more preferably 5×1017/cm3 or lower.
- In the case where the band gap (Eg) of an oxide semiconductor is 3.15 eV, the electron affinity (χ) is said to be 4.3 eV. The work function of titanium (Ti) included in the source electrode and the drain electrode is substantially equal to the electron affinity (χ) of the oxide semiconductor. In that case, a Schottky barrier for electrons is not formed at an interface between the metal and the oxide semiconductor.
- In other words, in the case where the work function of metal (φM) and the electron affinity (χ) of the oxide semiconductor are equal to each other and the metal and the oxide semiconductor are in contact with each other, an energy band diagram (a schematic diagram) like
FIG. 13A is obtained. - In
FIG. 13B , a black circle () represents an electron, and when a positive potential is applied to the drain, the electron is injected into the oxide semiconductor over the barrier (h) and flows toward the drain. In this case, the height of the barrier (h) changes depending on the gate voltage and the drain voltage; in the case where a positive drain voltage is applied, the height of the barrier (h) is smaller than the height of the barrier inFIG. 13A where no voltage is applied, i.e., ½ of the band gap (Eg). - At this time, the electron injected into the oxide semiconductor flows through the oxide semiconductor as illustrated in
FIG. 14A . In addition, inFIG. 14B , when a negative potential (reverse bias) is applied to the gate electrode (G1), the value of current is extremely close to zero because holes that are minority carriers are substantially zero. - By increasing the purity of the oxide semiconductor so that the oxide semiconductor does not include an impurity other than a main component thereof as much as possible, an intrinsic (i-type) or substantially intrinsic oxide semiconductor is obtained. Consequently, the interface characteristics with the gate insulating film become apparent. Therefore, the interface characteristics need to be considered separately from bulk characteristics.
- Accordingly, an insulating film formed using high-density plasma, according to an embodiment of the present invention, is preferably used as the gate insulating film in order to form a favorable interface with the oxide semiconductor.
- By increasing the purity of an oxide semiconductor and forming a favorable interface between the oxide semiconductor and a gate insulating film, even an element with a channel width W of 1×104 μm and a channel length of 3 μm is highly expected to have the following characteristics of a thin film transistor: the off current is 10−13 A or less, and the subthreshold swing (S value) is 0.1 V/dec. (the thickness of the gate insulating film: 100 nm).
- This embodiment can be combined with any of the other embodiments as appropriate.
- In this embodiment, as an example of a mode using high-density plasma, a structure of a microwave plasma CVD apparatus and specific deposition treatment of a gate insulating film will be described with reference to
FIG. 2 andFIG. 3 . -
FIG. 2 is a top view illustrating an example of a microwave plasma apparatus. Acommon chamber 1120 is connected to load/unload (L/UL)chambers gate valves 1122 to 1127. Asubstrate 1130 is set in acassette 1128 of the load/unload (L/UL)chamber 1110 or acassette 1129 of the load/unload (L/UL)chamber 1115 and transferred to the reaction chambers by atransfer unit 1121 of thecommon chamber 1120. - In
FIG. 2 , the microwave plasma CVD apparatus is provided with a plurality of load/unload (L/UL) chambers but may be provided with only one load/unload (L/UL) chamber. In addition, the high-density plasma CVD apparatus may be provided with a pretreatment chamber. By pre-heating the substrate in the pretreatment chamber, heating time before deposition in each reaction chamber can be shortened; accordingly, the throughput can be improved. -
FIG. 3 illustrates a detailed structure of a reaction chamber of the microwave plasma CVD apparatus used for forming a gate insulating film. - The reaction chamber of the microwave plasma CVD apparatus includes a
treatment container 180, asupport 181 which is provided in thetreatment container 180 and on which thesubstrate 1130 is set, anexhaust port 183 connected to a vacuum pump for exhausting a gas in thetreatment container 180, amicrowave generation unit 184 for supplying microwaves for generating plasma, awaveguide 185 for introducing microwaves from a microwave supply unit to thetreatment container 180, atop plate 187 which is in contact with thewaveguide 185 and hasopenings 187 a, and a plurality ofdielectric plates 186 fixed to thetop plate 187 with a fixingmember 188. Thesubstrate 1130 is provided to face thedielectric plates 186. As the vacuum pump, a dry pump for low vacuum evacuation and a turbo molecular pump for high vacuum evacuation can be used. In this embodiment, a substrate having a size of 600 mm×720 mm is used as thesubstrate 1130. Note that there is no limitation on the size of the substrate. - Further, a
gas pipe 197 through which a non-source gas flows and agas pipe 198 through which a source gas flows are provided between thesubstrate 1130 and thedielectric plates 186. Thegas pipe 197 through which a non-source gas flows is connected to a non-sourcegas supply source 191 via avalve 195 and amass flow controller 193. Thegas pipe 198 through which a source gas flows is connected to a sourcegas supply source 192 via avalve 196 and amass flow controller 194. - By provision of a
temperature control portion 199 for thesupport 181, the temperature of thesubstrate 1130 can be controlled. A high-frequency power source may be connected to thesupport 181, so that predetermined bias voltage is applied to thesupport 181 by AC electric power output from the high-frequency power source. Note that themicrowave generation unit 184 is preferably provided outside thetreatment container 180. - The
microwave generation unit 184 supplies microwaves. When the plurality ofmicrowave generation units 184 is provided, stable large-sized plasma can be generated. Therefore, a highly uniform film can be formed over a large-sized substrate with one side of over 600 mm, particularly over 1000 mm, and the deposition rate can be increased. - The
treatment container 180 and thetop plate 187 are formed using metal whose surface is covered with an insulating film of alumina, silicon oxide, or a fluorine resin, for example, an alloy including aluminum. Further, the fixingmember 188 is formed using metal such as an alloy including aluminum. - The
dielectric plates 186 are provided so as to be in close contact with the openings of thetop plate 187. The microwaves generated in themicrowave generation unit 184 are propagated to thedielectric plates 186 by passing through thewaveguide 185 and theopenings 187 a of thetop plate 187 and transmitted through thedielectric plates 186 to be released into the treatment container. - By field effect energy of the microwaves released into the treatment container, the non-source gas is excited into a plasma state. This
plasma 200 has higher density on the surface of thedielectric plates 186; thus, damage to thesubstrate 1130 can be reduced. - By provision of the plurality of
dielectric plates 186, uniform large-sized plasma can be generated and maintained. Thedielectric plates 186 are formed using ceramics such as sapphire, quartz glass, alumina, silicon oxide, or silicon nitride. - The
dielectric plates 186 may have a recessedportion 189 on the side where theplasma 200 is generated. With the recessedportion 189, stable plasma can be generated. Furthermore, by provision of the plurality ofdielectric plates 186, a highly uniform film can be formed over a large-sized substrate with one side of over 600 mm, particularly over 1000 mm, and the deposition rate can be increased. - The non-source gas flows through the plurality of
gas pipes 197 on the upper side, and the source gas flows through the plurality ofgas pipes 198 on the lower side. Thegas pipes gas pipes 197 through which the non-source gas flows are provided on thedielectric plates 186 side, and outlets of thegas pipes 198 through which the source gas flows are provided on thesubstrate 1130 side. When the plurality ofgas pipes 197 and the plurality ofgas pipes 198 are provided to intersect with each other, the distance between the gas pipes can be shortened and thus the distance between the outlets can be shortened; accordingly, deposition can be uniformly performed over thesubstrate 1130. This structure is particularly effective when a large-sized substrate is used. - By ejecting the non-source gas toward the
dielectric plates 186, theplasma 200 can be generated while a film is prevented from being formed on the surface of thedielectric plates 186. Further, since the source gas is ejected toward thesubstrate 1130, the source gas can be ejected from a position closer to thesubstrate 1130, and thus the deposition rate can be increased. Note that part of the source gas can flow through thegas pipes 197 on the upper side. - The
gas pipes gas pipes dielectric plates 186. - Deposition treatment of the
gate insulating film 102 is described below. - First, the deposition treatment starts at a step S170 in
FIG. 4 . The temperature of thesubstrate 1130 is controlled at a step S171. Thesubstrate 1130 is at room temperature or heated to 100° C. to 550° C. by thetemperature control portion 199. - At a step S172, the inside of the
treatment container 180 is made into a vacuum state, and one or more rare gases such as helium, argon, xenon, and krypton are introduced into thetreatment container 180 as a gas for generating plasma. When oxygen is introduced into thetreatment container 180 together with the rare gas, plasma can be easily generated. Note that the distance between thesubstrate 1130 and thedielectric plates 186 is approximately 10 mm to 200 mm (preferably 110 mm to 160 mm). - Next, at a step S173, the pressure in the
treatment container 180 is set at predetermined pressure, 1 Pa to 200 Pa, preferably 1 Pa to 100 Pa, more preferably 1 Pa to 40 Pa. - Then, at a step S174, the
microwave generation unit 184 is turned on, and microwaves are supplied from themicrowave generation unit 184 to thewaveguide 185, so that plasma is generated in thetreatment container 180. The output power of the microwave generation unit is set at 500 W to 6000 W, preferably 4000 W to 6000 W. By excitation of plasma by introducing the microwaves, plasma with low electron temperature (higher than or equal to 0.7 eV and lower than or equal to 3 eV, preferably higher than or equal to 0.7 eV and lower than or equal to 1.5 eV) and high electron density (1×1011 atoms/cm3 to 1×1013 atoms/cm3) can be generated. - Next, at a step S175, a source gas is introduced from the
gas pipes 198 into thetreatment container 180. Specifically, supply of oxygen is halted, and dinitrogen monoxide, a rare gas, and silicon hydride or silicon halide are introduced as a source gas, whereby a silicon oxynitride film can be formed over thesubstrate 1130. - Then, at a step S176, supply of the source gas is halted, the pressure in the treatment container is lowered, and the microwave generation unit is turned off, so that the deposition process finishes at a step S177.
- In the above method for deposition treatment of a silicon oxynitride film, a silicon oxynitride film which withstands high voltage can be formed under the following conditions: the substrate temperature is 300° C. to 350° C.; and the flow rate of dinitrogen monoxide is greater than or equal to 10 times and less than or equal to 300 times, preferably greater than or equal to 50 times and less than or equal to 200 times, of that of silicon hydride or silicon halide. In addition, the withstand voltage of the silicon oxynitride film can be increased under the following conditions: 2 to 6 microwave generation units with power of 5 kW are used; the pressure in the treatment container is 10 Pa to 100 Pa, preferably 10 Pa to 50 Pa; and the distance between the
substrate 1130 and thedielectric plates 186 is greater than or equal to 110 mm and less than or equal to 160 mm. -
FIG. 16 is a plain view illustrating an example of a structure of thewaveguide 185. Thewaveguide 185 extends in parallel with thetop plate 187, and the plurality ofwaveguides 185 is provided in parallel with each other. Thedielectric plates 186 are provided on thetop plate 187 in a matrix form. Thewaveguides 185 and theopenings 187 a formed in thetop plate 187 are provided to be aligned with thedielectric plates 186. When the substrate to be processed has a large area (e.g., when a glass substrate of 730 mm×920 mm or a glass substrate which has one side exceeding 1 m is used), thewaveguide 185 is preferably divided into plural parts and microwaves are supplied.FIG. 16 illustrates a structure in which branch waveguides are used at an end portion of eachwaveguide 185, and the microwaves divided into a plurality are supplied. A microwave power supply is connected to the tip of each branch waveguide. Use of a plurality of microwave power supplies makes it possible to keep uniformity of plasma even when the area of the substrate to be processed becomes large. - Although a silicon oxynitride film is formed as the gate insulating film in this embodiment, a silicon nitride film can also be formed. In that case, silane and nitrogen can be used as a source gas.
-
FIG. 10A shows the characteristics of a thin film transistor whose gate insulating film is formed with the microwave plasma CVD apparatus described in this embodiment, andFIG. 10B shows the characteristics of a thin film transistor whose gate insulating film is formed with a conventional plasma CVD apparatus. The results are compared with each other. - When the two thin film transistors are compared, especially in a gate bias-temperature (BT) test, the amount of threshold voltage (Vth) shift in the thin film transistor formed by the conventional method (
FIG. 10B ) is more than ±1.0, while the amount of threshold voltage (Vth) shift in the thin film transistor of this embodiment (FIG. 10A ) is reduced to lower than ±1.0. Thus, the reliability is largely improved. Here, the gate BT test is a test for evaluating the reliability of a transistor from the amount of shift in threshold voltage (Vth) or the like. The smaller the shift amount is, the more stable the operation of a transistor is and the higher the reliability thereof is. - Moreover, as for threshold voltage (Vth), the thin film transistor formed by the conventional method (
FIG. 10B ) is normally on and variation in a substrate surface is ±4.2 V, while the thin film transistor of this embodiment (FIG. 10A ) is normally off and variation in a substrate surface is largely reduced to ±1.0 V. - As described above, by forming a gate insulating film with use of a microwave plasma CVD apparatus, dangling bonds in the gate insulating film are reduced and the interface between the gate insulating film and an oxide semiconductor can be favorable. Accordingly, the characteristics of a manufactured thin film transistor can be improved.
- This embodiment can be combined with any of the other embodiments as appropriate.
- In this embodiment, an example of a structure of a microwave plasma CVD apparatus, which is different from that of
Embodiment 2, will be described with reference toFIG. 5 . - In
Embodiment 2, the source gas ejected from thegas pipes 198 on the lower side is blown up by the non-source gas ejected from thegas pipes 197 on the upper side as illustrated inFIG. 3 . The blown source gas is deposited on thedielectric plates 186 or the like as powder or a film. The deposited powder or film might fall onto thesubstrate 1130 over time and cause a particle. In this embodiment, a structure with which particles are reduced is described. - A reaction chamber illustrated in
FIG. 5 includes, instead of thegas pipes 197 on the upper side inFIG. 3 , a plurality of members 300 (also referred to as beams) provided in parallel with thedielectric plates 186. Gas outlets of themembers 300 are provided on thesubstrate 1130 side and eject a non-source gas. In addition, gas outlets of thegas pipes 198 provided between thesubstrate 1130 and thedielectric plates 186 are provided on thesubstrate 1130 side and eject a source gas. That is, both thegas pipes 198 and themembers 300 eject the gasses to thesubstrate 1130 side. - Note that the outlets of the
members 300 are connected to the non-sourcegas supply source 191 via a gas pipe inside the apparatus, thevalve 195, and themass flow controller 193. Further, thegas pipes 198 through which the source gas flows are connected to the sourcegas supply source 192 via thevalve 196 and themass flow controller 194. Note that a structure in which part of the source gas is ejected from themembers 300 can also be employed. - Further, the
gas pipes 198 are preferably provided to intersect with themembers 300 having the outlets. As illustrated inFIG. 5 , when the plurality ofgas pipes 198 and the plurality ofmembers 300 are provided to intersect with each other, the distance between themembers 300 and the distance between thegas pipes 198 can be shortened and thus the distance between the outlets can be shortened; accordingly, deposition can be uniformly performed over thesubstrate 1130. This structure is particularly effective when a large-sized substrate is used. It is also effective that the outlets of themembers 300 do not overlap with thegas pipes 198. If they overlap with each other, the gas ejected from themembers 300 might be blown up. - When both the source gas and the non-source gas are ejected to the
substrate 1130 side as in this embodiment, the source gas can be prevented from being blown up and generation of particles can be suppressed. The structure of this embodiment is particularly effective when the flow rate ratio of dinitrogen monoxide to silane is high, because particles are easily generated under such a condition. - With the structure of this embodiment, the characteristics of a thin film transistor described in
Embodiment 2 can be obtained, and further, the yield can be largely improved. - This embodiment can be combined with any of the other embodiments as appropriate.
- In this embodiment, an example of a bottom-gate thin film transistor having a channel-etched structure, which is different from that of Embodiment 1, will be described with reference to
FIG. 6 . - The thin film transistor is manufactured by sequentially forming the
gate electrode 101, thegate insulating film 102, theoxide semiconductor film 108, thesource electrode 106 and thedrain electrode 107, the insulatingfilm 109, aback-gate electrode 601, and an insulatingfilm 602 over thesubstrate 100 with an insulating property. - In order to form the
gate insulating film 102, the microwave plasma CVD apparatus described inEmbodiment 2 or 3 can be used. Dangling bonds in thegate insulating film 102 can be reduced and the interface between theoxide semiconductor film 108 and thegate insulating film 102 can be favorable. - The
back-gate electrode 601 is formed in a position overlapping with theoxide semiconductor film 108 in such a manner that a conductive film is formed over the insulatingfilm 109 and then the conductive film is patterned. Theback-gate electrode 601 can be formed using a material and a structure similar to those of thegate electrode 101, or thesource electrode 106 and thedrain electrode 107. - The thickness of the
back-gate electrode 601 is 10 nm to 400 nm, preferably 100 nm to 200 nm. In this embodiment, a conductive film having a structure in which a titanium film, an aluminum film, and a titanium film are stacked is formed. Then, a resist mask is formed by a photolithography method, and an unnecessary portion is removed by etching so that the conductive film is processed (patterned) into a desired shape; thus, theback-gate electrode 601 is formed. - The insulating
film 602 is preferably formed using a material with a high barrier property that can prevent moisture, hydrogen, oxygen, and the like in an atmosphere from affecting the characteristics of the transistor. For example, the insulating film can be formed to have a single-layer structure or a stacked-layer structure using an insulating film with a high barrier property such as a silicon nitride film, a silicon nitride oxide film, an aluminum nitride film, or an aluminum nitride oxide film by a plasma CVD method, a sputtering method, or the like. In order to obtain an effect of a barrier property, the insulatingfilm 602 is preferably formed to a thickness of 15 nm to 400 nm, for example. - Note that the
back-gate electrode 601 may be electrically insulated and in a floating state, or may be supplied with a potential. In the latter case, theback-gate electrode 601 may be supplied with the same potential as thegate electrode 101, or may be supplied with a fixed potential such as a ground potential. By controlling the level of a potential supplied to theback-gate electrode 601, the threshold voltage of the transistor is controlled; consequently, variation in the threshold voltage in a substrate surface can be reduced. - In
FIGS. 11A and 11B , the characteristics of a thin film transistor provided with a back-gate electrode and those of a thin film transistor without a back-gate electrode are compared. -
FIG. 11A shows the results in the case of forming a back-gate electrode as in this embodiment.FIG. 11B shows the results in the case of not forming a back-gate electrode as in Embodiment 1 (which is the same asFIG. 10A ). - When the two thin film transistors are compared, variation in the threshold voltage (Vth) in a substrate surface of the thin film transistor provided with the back-gate electrode (
FIG. 11A ) is largely reduced to ±0.5 V. Therefore, with a back-gate electrode, the characteristics of a thin film transistor can be further improved. - This embodiment can be combined with any of the other embodiments as appropriate.
- In this embodiment, a bottom-gate thin film transistor having a channel protective structure will be described with reference to
FIG. 7 . -
FIG. 7 illustrates an example of a cross-sectional structure of a bottom-gate thin film transistor having a channel protective structure. - The thin film transistor is manufactured by sequentially forming the
gate electrode 101, thegate insulating film 102, theoxide semiconductor film 104, a channelprotective film 701, thesource electrode 106 and thedrain electrode 107, and the insulatingfilm 109 over thesubstrate 100 with an insulating property. - The channel
protective film 701 is formed over theoxide semiconductor film 104 so as to overlap with a channel formation region of theoxide semiconductor film 104. The channelprotective film 701 can prevent the portion of theoxide semiconductor film 104, which serves as the channel formation region, from being damaged in a later step (e.g., reduction in thickness due to plasma or an etchant in etching). Therefore, the reliability of the thin film transistor can be improved. - The channel
protective film 701 can be formed using an inorganic material including oxygen (such as silicon oxide, silicon oxynitride, or silicon nitride oxide). - Here, in order to form the
gate insulating film 102, the microwave plasma CVD apparatus described inEmbodiment 2 or 3 can be used. Dangling bonds in thegate insulating film 102 can be reduced and the interface between theoxide semiconductor film 104 and thegate insulating film 102 can be favorable. - This embodiment can be combined with any of the other embodiments as appropriate.
- In this embodiment, a top-gate thin film transistor will be described with reference
FIG. 8 . -
FIG. 8 illustrates an example of a cross-sectional structure of a top-gate thin film transistor. - The thin film transistor is manufactured by sequentially forming an insulating
film 801, anoxide semiconductor film 802, asource electrode 803 and adrain electrode 804, agate insulating film 805, and agate electrode 806 over asubstrate 800 having an insulating surface. - In order to form the
gate insulating film 805, the microwave plasma CVD apparatus described inEmbodiment 2 or 3 can be used. Dangling bonds in thegate insulating film 805 can be reduced and the interface between theoxide semiconductor film 802 and thegate insulating film 805 can be favorable. - This embodiment can be combined with any of the other embodiments as appropriate.
- It is effective to use microwaves with a frequency of 1 GHz or lower in a microwave plasma CVD apparatus.
- By using the microwaves with a frequency of 1 GHz or lower, the uniformity of plasma in a reaction chamber can be maintained even when the kind of gasses is changed or the pressure is changed in a wide range. The frequency is preferably 915 MHz.
- In addition, when a structure like that in Embodiment 3, with which powder or a film of a source gas is prevented from being deposited in a reaction chamber, is employed, different films can be successively formed only by changing the kind of gasses. Therefore, it is particularly effective to combine the structure of this embodiment with the structure of Embodiment 3.
- This embodiment can be combined with any of the other embodiments as appropriate.
- In this embodiment, a gate insulating film having a structure different from that of other embodiments will be described. Any of the structures and manufacturing methods of other embodiments other than the gate insulating film can be applied to this embodiment.
- By increasing the thickness of a gate insulating film, leakage current can be reduced and the reliability of a semiconductor device can be improved.
- However, when the material of the gate insulating film described in Embodiment 1 is used, there is a possibility that the channel capacitance cannot be secured owing to increase in the thickness.
- In this embodiment, therefore, the gate insulating film has a stacked-layer structure of a first insulating film formed by microwave plasma CVD and a second insulating film with a higher dielectric constant than the first insulating film.
- At this time, the first insulating film formed by microwave plasma CVD is used as an insulating film that is in contact with an oxide semiconductor film, whereby the quality of the interface therebetween is improved. On the other hand, a thick insulating film with a higher dielectric constant than the first insulating film is used as the second insulating film that is not in contact with the oxide semiconductor, whereby the channel capacitance can be secured with leakage current suppressed.
- As the insulating film with a high dielectric constant, an oxide film, a nitride film, an oxynitride film, a nitride oxide film, or the like including hafnium (Hf), zirconium (Zr), lanthanum (La), or the like can be used. For example, a film of hafnium oxide or the like may be formed by a sputtering method. Even when the second insulating film is formed by a sputtering method, the first insulating film is provided between the second insulating film and the oxide semiconductor; therefore, the quality of the interface with the oxide semiconductor is improved.
- The gate insulating film of this embodiment may be applied to a bottom-gate transistor like that in
FIGS. 1A to 1E ,FIG. 6 , orFIG. 7 or may be applied to a top-gate transistor like that inFIG. 8 . - This embodiment can be combined with any of the other embodiments as appropriate.
- In this embodiment, examples of electronic devices will be described.
-
FIG. 9A illustrates an example of electronic paper (also referred to as an electronic book reader).FIG. 9B illustrates an example of a display device.FIG. 9C illustrates an example of a display device having flexibility.FIG. 9D illustrates an example of a portable game machine.FIG. 9E illustrates an example of a mobile phone. - In the electronic devices illustrated in
FIGS. 9A to 9E , a semiconductor device according to an embodiment of the present invention can be used fordisplay portions 7011 to 7015 provided formain bodies 7001 to 7005. Note that the semiconductor device according to an embodiment of the present invention can also be used for an electronic device which does not have a display portion. - This embodiment can be combined with any of the other embodiments as appropriate.
- This application is based on Japanese Patent Application serial no. 2009-255154 filed with Japan Patent Office on Nov. 6, 2009, the entire contents of which are hereby incorporated by reference.
Claims (16)
1. (canceled)
2. An oxide semiconductor film, wherein:
the oxide semiconductor film includes In, Ga, and Zn, and
a carrier concentration of the oxide semiconductor film is lower than 1×1014/cm3.
3. The oxide semiconductor film according to claim 2 , wherein hydrogen in the oxide semiconductor film is reduced, and then oxygen is introduced into a deficient portion from which the hydrogen is removed and an oxygen-deficient portion, whereby the carrier concentration of the oxide semiconductor film is lower than 1×1014/cm3.
4. The oxide semiconductor film according to claim 3 , wherein the hydrogen in the oxide semiconductor film is reduced by a heat treatment.
5. The oxide semiconductor film according to claim 2 , wherein a band gap of the oxide semiconductor film is 2 eV or more.
6. The oxide semiconductor film according to claim 3 , wherein the hydrogen in the oxide semiconductor film serves as a donor.
7. A semiconductor device comprising:
an oxide semiconductor film; and
an insulating film partly in contact with the oxide semiconductor film,
wherein:
the oxide semiconductor film includes In, Ga, and Zn,
a carrier concentration of the oxide semiconductor film is lower than 1×1014/cm3, and
the insulating film supplies oxygen to the oxide semiconductor film.
8. The semiconductor device according to claim 7 , wherein hydrogen in the oxide semiconductor film is reduced, and then oxygen is introduced into a deficient portion from which the hydrogen is removed and an oxygen-deficient portion, whereby the carrier concentration of the oxide semiconductor film is lower than 1×1014/cm3.
9. The semiconductor device according to claim 8 , wherein the hydrogen in the oxide semiconductor film is reduced by a heat treatment.
10. The semiconductor device according to claim 7 , wherein a band gap of the oxide semiconductor film is 2 eV or more.
11. The semiconductor device according to claim 8 , wherein the hydrogen in the oxide semiconductor film serves as a donor.
12. A semiconductor device comprising:
an oxide semiconductor film; and
an insulating film partly in contact with the oxide semiconductor film,
wherein:
the oxide semiconductor film includes In, Ga, and Zn,
a carrier concentration of the oxide semiconductor film is lower than 1×1014/cm3, and
an oxygen concentration of the insulating film is higher than that of the oxide semiconductor film.
13. The semiconductor device according to claim 12 , wherein hydrogen in the oxide semiconductor film is reduced, and then oxygen is introduced into a deficient portion from which the hydrogen is removed and an oxygen-deficient portion, whereby the carrier concentration of the oxide semiconductor film is lower than 1×1014/cm3.
14. The semiconductor device according to claim 13 , wherein the hydrogen in the oxide semiconductor film is reduced by a heat treatment.
15. The semiconductor device according to claim 12 , wherein a band gap of the oxide semiconductor film is 2 eV or more.
16. The semiconductor device according to claim 13 , wherein the hydrogen in the oxide semiconductor film serves as a donor.
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JP2011119719A (en) | 2011-06-16 |
JP2017034268A (en) | 2017-02-09 |
TW201628097A (en) | 2016-08-01 |
JP6207018B2 (en) | 2017-10-04 |
TW201135848A (en) | 2011-10-16 |
JP2014103415A (en) | 2014-06-05 |
KR20120093327A (en) | 2012-08-22 |
US20110111557A1 (en) | 2011-05-12 |
WO2011055644A1 (en) | 2011-05-12 |
KR101930230B1 (en) | 2018-12-18 |
US8927351B2 (en) | 2015-01-06 |
US9384976B2 (en) | 2016-07-05 |
US20150140732A1 (en) | 2015-05-21 |
KR101747158B1 (en) | 2017-06-14 |
TWI619175B (en) | 2018-03-21 |
TWI539526B (en) | 2016-06-21 |
KR20170056709A (en) | 2017-05-23 |
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