WO2006132379A2 - Structure for functional film pattern formation and method of manufacturing functional film - Google Patents
Structure for functional film pattern formation and method of manufacturing functional film Download PDFInfo
- Publication number
- WO2006132379A2 WO2006132379A2 PCT/JP2006/311666 JP2006311666W WO2006132379A2 WO 2006132379 A2 WO2006132379 A2 WO 2006132379A2 JP 2006311666 W JP2006311666 W JP 2006311666W WO 2006132379 A2 WO2006132379 A2 WO 2006132379A2
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- WIPO (PCT)
- Prior art keywords
- functional film
- layer
- separation layer
- substrate
- manufacturing
- Prior art date
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- 238000004519 manufacturing process Methods 0.000 title claims abstract description 63
- 230000007261 regionalization Effects 0.000 title claims description 39
- 239000000758 substrate Substances 0.000 claims abstract description 155
- 239000000463 material Substances 0.000 claims abstract description 118
- 238000000926 separation method Methods 0.000 claims abstract description 114
- 238000010438 heat treatment Methods 0.000 claims abstract description 35
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 20
- 239000013078 crystal Substances 0.000 claims description 20
- 239000012298 atmosphere Substances 0.000 claims description 18
- 239000004065 semiconductor Substances 0.000 claims description 13
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 12
- 239000011521 glass Substances 0.000 claims description 12
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 10
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 10
- 239000000919 ceramic Substances 0.000 claims description 10
- NLSCHDZTHVNDCP-UHFFFAOYSA-N caesium nitrate Chemical compound [Cs+].[O-][N+]([O-])=O NLSCHDZTHVNDCP-UHFFFAOYSA-N 0.000 claims description 9
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 9
- 239000000853 adhesive Substances 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- -1 transition metal chalcogenide Chemical class 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 claims description 6
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 6
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 claims description 6
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 claims description 6
- 150000004767 nitrides Chemical class 0.000 claims description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 6
- 229910000018 strontium carbonate Inorganic materials 0.000 claims description 6
- UBXAKNTVXQMEAG-UHFFFAOYSA-L strontium sulfate Chemical compound [Sr+2].[O-]S([O-])(=O)=O UBXAKNTVXQMEAG-UHFFFAOYSA-L 0.000 claims description 6
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 6
- 229910000368 zinc sulfate Inorganic materials 0.000 claims description 6
- 229910052582 BN Inorganic materials 0.000 claims description 5
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 5
- 229910002651 NO3 Inorganic materials 0.000 claims description 5
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 claims description 5
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 claims description 5
- 229910052808 lithium carbonate Inorganic materials 0.000 claims description 5
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims description 5
- 239000007769 metal material Substances 0.000 claims description 5
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 claims description 5
- 229910052982 molybdenum disulfide Inorganic materials 0.000 claims description 5
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 claims description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- 238000003776 cleavage reaction Methods 0.000 claims description 4
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 4
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 4
- 239000000696 magnetic material Substances 0.000 claims description 4
- 229910052976 metal sulfide Inorganic materials 0.000 claims description 4
- 230000007017 scission Effects 0.000 claims description 4
- KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 claims description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052924 anglesite Inorganic materials 0.000 claims description 3
- 229910052925 anhydrite Inorganic materials 0.000 claims description 3
- 229910000380 bismuth sulfate Inorganic materials 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052923 celestite Inorganic materials 0.000 claims description 3
- KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 claims description 3
- BEQZMQXCOWIHRY-UHFFFAOYSA-H dibismuth;trisulfate Chemical compound [Bi+3].[Bi+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BEQZMQXCOWIHRY-UHFFFAOYSA-H 0.000 claims description 3
- 229910002804 graphite Inorganic materials 0.000 claims description 3
- 239000010439 graphite Substances 0.000 claims description 3
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 claims description 3
- 239000001095 magnesium carbonate Substances 0.000 claims description 3
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 3
- 239000010445 mica Substances 0.000 claims description 3
- 229910052618 mica group Inorganic materials 0.000 claims description 3
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 3
- 229910052723 transition metal Inorganic materials 0.000 claims description 3
- 229960001763 zinc sulfate Drugs 0.000 claims description 3
- 239000011686 zinc sulphate Substances 0.000 claims description 3
- 229910010272 inorganic material Inorganic materials 0.000 claims 8
- 239000011147 inorganic material Substances 0.000 claims 8
- 235000019341 magnesium sulphate Nutrition 0.000 claims 2
- 238000000034 method Methods 0.000 abstract description 48
- 230000015572 biosynthetic process Effects 0.000 abstract description 28
- 230000008569 process Effects 0.000 abstract description 24
- 239000010408 film Substances 0.000 description 143
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 19
- 239000007789 gas Substances 0.000 description 15
- 229910052454 barium strontium titanate Inorganic materials 0.000 description 12
- 230000006870 function Effects 0.000 description 12
- 239000010936 titanium Substances 0.000 description 11
- 239000010409 thin film Substances 0.000 description 10
- 238000000354 decomposition reaction Methods 0.000 description 9
- 238000004544 sputter deposition Methods 0.000 description 9
- 239000003990 capacitor Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 238000005516 engineering process Methods 0.000 description 8
- 239000010453 quartz Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 229910052719 titanium Inorganic materials 0.000 description 8
- 238000000151 deposition Methods 0.000 description 7
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 238000005229 chemical vapour deposition Methods 0.000 description 5
- 229910052746 lanthanum Inorganic materials 0.000 description 5
- 229910052697 platinum Inorganic materials 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 239000003989 dielectric material Substances 0.000 description 3
- 238000001312 dry etching Methods 0.000 description 3
- 239000000395 magnesium oxide Substances 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 3
- 239000008204 material by function Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000005368 silicate glass Substances 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 229910021417 amorphous silicon Inorganic materials 0.000 description 2
- 238000004380 ashing Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000013590 bulk material Substances 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 229910052593 corundum Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052596 spinel Inorganic materials 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- 229910001845 yogo sapphire Inorganic materials 0.000 description 2
- 229910021521 yttrium barium copper oxide Inorganic materials 0.000 description 2
- WSMQKESQZFQMFW-UHFFFAOYSA-N 5-methyl-pyrazole-3-carboxylic acid Chemical compound CC1=CC(C(O)=O)=NN1 WSMQKESQZFQMFW-UHFFFAOYSA-N 0.000 description 1
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 description 1
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910002601 GaN Inorganic materials 0.000 description 1
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 description 1
- GPXJNWSHGFTCBW-UHFFFAOYSA-N Indium phosphide Chemical compound [In]#P GPXJNWSHGFTCBW-UHFFFAOYSA-N 0.000 description 1
- 229910003327 LiNbO3 Inorganic materials 0.000 description 1
- 229910026161 MgAl2O4 Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- GPBUGPUPKAGMDK-UHFFFAOYSA-N azanylidynemolybdenum Chemical compound [Mo]#N GPBUGPUPKAGMDK-UHFFFAOYSA-N 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 238000000609 electron-beam lithography Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000005355 lead glass Substances 0.000 description 1
- GQYHUHYESMUTHG-UHFFFAOYSA-N lithium niobate Chemical compound [Li+].[O-][Nb](=O)=O GQYHUHYESMUTHG-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910052961 molybdenite Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 238000005546 reactive sputtering Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229940001593 sodium carbonate Drugs 0.000 description 1
- 238000003980 solgel method Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- LEDMRZGFZIAGGB-UHFFFAOYSA-L strontium carbonate Chemical compound [Sr+2].[O-]C([O-])=O LEDMRZGFZIAGGB-UHFFFAOYSA-L 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/76—Making of isolation regions between components
- H01L21/762—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers
- H01L21/7624—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using semiconductor on insulator [SOI] technology
- H01L21/76251—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using semiconductor on insulator [SOI] technology using bonding techniques
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/20—Deposition of semiconductor materials on a substrate, e.g. epitaxial growth solid phase epitaxy
- H01L21/2003—Deposition of semiconductor materials on a substrate, e.g. epitaxial growth solid phase epitaxy characterised by the substrate
- H01L21/2007—Bonding of semiconductor wafers to insulating substrates or to semiconducting substrates using an intermediate insulating layer
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/01—Manufacture or treatment
- H10N30/07—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base
- H10N30/072—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by laminating or bonding of piezoelectric or electrostrictive bodies
- H10N30/073—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by laminating or bonding of piezoelectric or electrostrictive bodies by fusion of metals or by adhesives
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/01—Manufacture or treatment
- H10N30/07—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base
- H10N30/074—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by depositing piezoelectric or electrostrictive layers, e.g. aerosol or screen printing
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N60/00—Superconducting devices
- H10N60/01—Manufacture or treatment
- H10N60/0268—Manufacture or treatment of devices comprising copper oxide
- H10N60/0296—Processes for depositing or forming copper oxide superconductor layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
- H01L21/02172—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing at least one metal element, e.g. metal oxides, metal nitrides, metal oxynitrides or metal carbides
- H01L21/02197—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing at least one metal element, e.g. metal oxides, metal nitrides, metal oxynitrides or metal carbides the material having a perovskite structure, e.g. BaTiO3
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/314—Inorganic layers
- H01L21/316—Inorganic layers composed of oxides or glassy oxides or oxide based glass
- H01L21/31691—Inorganic layers composed of oxides or glassy oxides or oxide based glass with perovskite structure
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/14—Layer or component removable to expose adhesive
- Y10T428/1486—Ornamental, decorative, pattern, or indicia
Definitions
- the present: invention relates to a method of manufacturing a functional film including a dielectric material, piezoelectric material, pyroelectric material, magnetic material, semiconductor material or the like, and specifically to amethod of manufacturing the functional film having a pattern . Further, the present invention relates to a structure for functional film pattern formation to be used in a manufacturing process of the functional film.
- a filmof functionalmaterial also simply referred to as "functional film”
- a functional film layer is formed on a substrate
- a mask pattern is formed by applying a resist onto the film and performing exposure to light and development thereon
- the functional film layer is dry etchedor wet etched, and thereby, a functional film pattern is obtained.
- the functional film formed by film formation does not sufficiently exert its function in a condition after the film formation, and the film is inferior to a bulk material in performance . Accordingly, in order to sufficiently express the function of a functional film, heat treatment at relatively high temperature (e.g., about 500 0 C to 1000 0 C) is required after film formation.
- relatively high temperature e.g., about 500 0 C to 1000 0 C
- Japanese Patent Application Publication JP-P2005-64289A discloses a method for forming a high-density micropattern.
- the method includes the steps of forming an organicmonomolecular film on a first substrate, microfabricating the organic monomolecular film by photolithography to form an organic monomolecular film pattern, selectively growing a thin film on the organic monomolecular film pattern, and transferring the thin film onto a second substrate to form a micropattern of the thin film on the second substrate (page 2) .
- the patterned functional film (the thin film 15 shown in Fig. 4 of JP-P2005-64289A) can be transferred relatively easily.
- the organicmonomolecular film is usedin thismethod, and therefore, it is impossible to form the functional film by a high-temperature process nor perform high-temperature heat treatment on the formed functional film.
- a firstpurpose of the present invention is to provide amethod of manufacturing a functional film by which a fine pattern can be formed. Further, a second purpose of the present invention is to provide amethod ofmanufacturing a functional film by which a functional film formed through a high temperature process can be provided on a desired substrate. Furthermore, a third purpose of the present invention is to provide a structure for functional film pattern formation to be used in a manufacturing process of such a functional film.
- a structure for functional film pattern formation includes : a substrate in which a predetermined pattern is formed; a separation layer directly or indirectly provided on the substrate; and a layer to be peeled provided on the separation layer and containing a functional filmformedbyusing a functionalmaterial , wherein the layer to be peeled is peeled from the substrate or bonding strength between the layer to be peeled and the substrate becomes lower by heating the separation layer, applying an electromagnetic wave toward the separation layer, or applying an external force to the separation layer.
- a method of manufacturing a function film includes the steps of: (a) preparing a substrate in which a predetermined pattern is formed; (b) forming a separation layer directly or indirectly on the substrate; (c) forming a layer to be peeled containing a functional film, which is formed by using a functional material , on the separation layer; and (d) peeling the layer to be peeled from the substrate or reducing bonding strength between the layer to be peeled and the substrate by heating the separation layer, applying an electromagnetic wave toward the separation layer, or applying an external force to the separation layer.
- reaction refers to a process in which, from one material or material system, another material or material system different from the initial material or material system in composition or structure is produced.
- reaction includes a process in which one kind of compound changes into two or more kinds of simplermaterials , and a process in which, based on two kinds of materials including at least one kind of compound, two or more kinds of materials different from the initial materials are produced.
- the former case is specifically referred to as “decomposition”
- the decomposition brought about by heating is referred to as “thermal decomposition” .
- the functional film is formed on the substrate in which the pattern has been formed in advance, and thereby, the process of performing dry etching orwetetchingon the functional film canbe omitted.
- the functional film is formed on the substrate via the separation layer, and therefore, by applying heat, an electromagnetic wave or an external force to the layer to be peeled, the substrate and the functional film can be easily peeled, or the bonding strength between them is reduced such that they can be dynamically and easily peeled at the subsequent step.
- the fine functional film pattern formed through the high temperature process can be easily transferred to a flexible substrate, for example, having relatively low heat tolerance and utilized. Therefore, elements having advantageous properties can be suitably mounted on instruments according to application and the performance of the entire instruments utilizing such elements can be improved.
- Fig. 1 is a flowchart showing a method of manufacturing a functional film according to the first to third embodiments of the present invention.
- Figs . 2A to 2F are sectional views for explanation of the method of manufacturing a functional film according to • the first embodiment of the present invention.
- Figs. 3A to 3C are sectional views for explanation of the method of manufacturing a functional film according to the second embodiment of the present invention.
- Figs . 4A and 4B are sectional views for explanation of amodified example of the method of manufacturing a functional film according to the second embodiment of the present invention.
- Figs . 5A to 5C are sectional views for explanation of the method of manufacturing a functional film according to the third embodiment of the present invention.
- Fig. 6 is a sectional view showing a modified example of a structure for functional film pattern formation.
- Fig. 7 is a sectional view showing another modified example of the structure for functional film pattern formation.
- Fig. 1 is a flowchart showing a method of manufacturing a functional film according to the first to third embodiments of thepresent invention .
- Figs .2Ato 2Fare diagrams for explanation of the method of manufacturing a functional filmaccordingto the firstembodimentof thepresentinvention in which Figs . 2A to 2C show steps of fabricating a structure for functional film pattern formation according to the first embodiment of the present invention.
- a substrate (mold) 101, inwhichapatternhavingprojections anddepressions is formed, is prepared as shown in Fig. 2A.
- the projecting portions correspond to a pattern to be formed in a functional film as a target of manufacturing.
- a single crystal material including a semiconductor single crystal material and an oxide single crystal material, a ceramics material, a glass material, or a metal material may be used.
- the substrate material is selected in consideration of heat tolerance or the like to a process temperature in the film formation process when the functional film is formed and the heat treatment process performed according to need.
- magnesium oxide (MgO) magnesium oxide (MgO) , alumina (Al 2 O 3 ) , titanium oxide (TiO 2 ) , zinc oxide (ZnO) , spinel (magnesium aluminate, MgAl 2 O 4 ) , strontium titanate (SrTiO 3 ) , lanthanum aluminate (LaAlOs) , lithium niobate (LiNbO 3 ) , lithium tantalate (LiTaO 3 ) and so on are cited.
- MgO magnesium oxide
- TiO 2 titanium oxide
- ZnO zinc oxide
- spinel magnesium aluminate
- strontium titanate (SrTiO 3 ) strontium titanate
- LaAlOs lanthanum aluminate
- LiNbO 3 lithium niobate
- LiTaO 3 lithium tantalate
- the oxide single crystal material by selecting a material having a predetermined lattice constant according to a functional film as a target ofmanufacturing, the functional filmcanbe formed by epitaxial growth. Further, since these materials are stable in an oxidizing atmosphere, they can be used for film formation or heat-treated at high temperature (e.g., about 1000 0 C for magnesium oxide) in the air atmosphere.
- a semiconductor single crystalmaterial specifically, silicon (Si) , germanium (Ge) , gallium arsenide (GaAs) ,
- GaP gallium phosphide
- InP indium phosphide
- the semiconductor single crystal material by selecting a material having a predetermined lattice constant according to a functional film as a target ofmanufacturing, the functional filmcanbe formed by epitaxial growth. Further, since these materials are stable in a reducing atmosphere, they can be used for film formation or heat-treated at high temperature (e.g. , about 1000 0 C for silicon) in the reducing atmosphere.
- alumina (Al 2 O 3 ) , zirconia (ZrO 2 ) , aluminumnitride (AlN) andso on are cited. Since the ceramics material is more inexpensive than the single crystalmaterial , thecostofmanufacturingcanbereduced. Further, sincethese materials are stable in the air atmosphere and have high heat tolerance, they canbe used for film formation or heat-treated at high temperature (e.g., about 1100 0 C for alumina) in the air atmosphere.
- silicate glass As a glass material, specifically, silicate glass, alkaline silicateglass, borosilicateglass , soda-limeglass , lead glass and so on are cited. Since the glass material is more inexpensive than the single crystal material, the cost of manufacturing can be reduced. Further, since these materials are stable in an oxidizing atmosphere, they can be used for film formation or heat-treated at high temperature
- metal such asplatinum
- metal material is more inexpensive than the single crystal material, the cost of manufacturing can be reduced. Further, since these materials are stable in a reducing atmosphere, they can be used for film formation or heat-treated at high temperature (e.g. , about 1000 0 C for platinum) in the reducing atmosphere.
- the substrate 101 can be fabricated by forming a pattern in a substrate made of the above-mentioned material by using dry etching, electron beam lithography or the like.
- a mold fabrication technology used in nanoimprint technology may be applied.
- a commercially available nanoimprint mold may be used.
- a separation layer 102 is formed on the substrate 101, as shown in Fig.2B.
- the separation layer 102 is a sacrifice layer that is removed when a functional film to be formed at the subsequent step is peeled from the substrate 101.
- a material of the separation layer 102 a material that induces a reaction of thermal decomposition or the like by being heated to generate a gas is used.
- metal nitride containing at least one element of Ti, V, Cr, Mh, Fe, Co, Ni, Ga gallium nitride is decomposed at about 900 0 C) , Zr, Mo (molybdenum nitride is decomposed at about 900 0 C) , Ta andW
- metal sulfide containing at least one element of V, Cr, Mn, Fe, Co, Ni, Mo, Ta and W, andmetal carbide such as TiC may be used.
- These compounds are applied with an electromagnetic wave having a predetermined wavelength to react with components in the atmosphere or an adjacent layer, i.e.
- components contained in the substrate 101 or a layer to be peeled 103 which will be described later, to generate a gas.
- the separation layer reacts with the oxide to generate nitrogen (N 2 ) .
- a known method such as spin coating, sputtering and CVD (chemical vapor deposition) methods may be used.
- a layer to be peeled 103 containing a material of a functional film as a target of manufacturing (functional material) is formed on the separation layer 102, as shown in Fig. 2C.
- the layer to be peeled 103 is formed by using a known method such as a sputtering method, a CVD method, a sol-gelmethodandanaerosol deposition (AD) method.
- the AD method is a film forming method of generating an aerosol in which raw material powder is dispersed in a gas, injecting the aerosol from a nozzle toward a substrate to allow the raw material powder to collide with the under layer, and thereby, depositing the raw material on the substrate, andthemethodis also called “injection deposition method” or “gas deposition method” .
- Pb (Zr,Ti) O 3 , SrBi 2 (Ta,Nb) 2 O 9 , Bi 4 Ti 3 Oi 2 and so on are cited.
- a material of a functional film to be used for a piezoelectric element such as an actuator
- Pb (Zr,Ti) O 3 Pb(Mgi /3 Nb 2/3 )O 3 , Pb(Zn i/3 Nb 2/3 )O 3 , Pb (Nii /3 Nb 2/3 )O 3 and so on, and solid solutions thereof are cited.
- a material of a functional film to be used for a pyroelectric element such as an infrared sensor
- Pb (Zr,Ti) O 3 , (Pb,La) (Zr,Ti) O 3 and so on are cited 1 .
- apassive component such as a capacitor
- SQUID superconducting quantum interference device
- a material of a functional film to be used for a photoelectric conversion element such as a solar cell amorphous silicon and compound semiconductor are cited.
- a material of a functional film to be used for a micro magnetic element such as a magnetic head, PdPtMn, CoPtCr and so on are cited.
- a material of a functional film to be used for a semiconductor element such as a TFT, amorphous silicon and so on are cited.
- the structure for functional film pattern formation includes the substrate 101, the separation layer 102 and the layer to be peeled 103 formed at those steps Sl to S3.
- a substrate for transfer104 isprepared, and the structure for functional film pattern formation 101 to 103 is provided and fixed such that'the layer to be peeled 103 faces the substrate for transfer 104, as shown in Fig. 2D .
- thelayertobepeeled.103 andthe substrate for transfer 104 maybe fixed to each otherby using an adhesive agentor the like .
- adesired substrate such as a synthesized resin substrate of epoxy or the like or glass substrate may be used. Further, electrodes and interconnections may be formed at the substrate for transfer 104 side in advance.
- step S5 heat treatment is performed on the structure for functional film pattern formation 101 to 103.
- the temperature of the heat treatment is set to the same level with the reaction temperature of the separation layer 102 or more in order to cause the reaction such as thermal composition or the like in the separation layer 102.
- reaction such as thermal decomposition occurs in the separation layer 102 and a gas is generated.
- Fig. 2F the layer to be peeled 103 is peeled from the substrate 101 and transferred to the substrate for transfer 104.
- the bonding strength between the layer to be peeled 103 and the substrate 101 becomes lower as a result ofgenerating the gas , andthereby, the layer to bepeeled 103 canbe dynamically and easilypeeled form the substrate 101.
- the layer to be peeled 103 can be transferred by peeling the substrate for transfer 104 at the same time as heating or at the subsequent step.
- step S5 heat treatment (post anneal) for
- ⁇ promoting grain growth in the functional film or improving crystallinity to improve the function of the film may be performed.
- heat treatment is performed at temperature of 500 0 C or more .
- SrBi 2 (Ta,Nb) 2 O 9 , Bi 4 Ti 3 Oi 2 , YBa 2 Cu 3 O 7 , Bi 2 Sr 2 Ca 2 Cu 3 Oi 0 Or the like heat treatment is performed at temperature of 700 0 C ormore . In this case, it is necessary to select thematerials of the substrate for transfer 104 and adhesive agent in consideration of heat tolerance to the heat treatment temperature .
- the functional film can be peeled from the substrate by heat treatment or they can be made easier to be peeled by reducing the bonding strength between them. Accordingly, a high-performance functional film fabricated by a film formation technology can be provided in a desired pattern on a desired substrate. Further, since the heat treatment process and the peeling (transfer) process can be performed at the same timeby selecting the appropriate separation layer material according to the heat treatment temperature and heat treatment atmosphere for the functional film, the manufacturing process becomes simpler and the cost of manufacturing can be reduced.
- Figs .3A to 3C are sectional views for explanation of the method of manufacturing a functional film according to the embodiment.
- the method of manufacturing a functional film according to the embodiment is characterized in that an electromagnetic wave is used at the step (S5) of peeling the layer to be peeled from the substrate .
- a structure for functional film pattern formation 201 to 203 including a substrate 201 , a separation layer 202 and a layer to be peeled 203 is fabricated, as shown in Fig. 3A.
- suitable one is selected from a single crystal material including a semiconductor single crystal material and an oxide single crystal material, a ceramics material and a glass material according to a wavelength of the electromagnetic wave to be used and so on .
- a single crystal material including a semiconductor single crystal material and an oxide single crystal material, a ceramics material and a glass material according to a wavelength of the electromagnetic wave to be used and so on .
- light such as ultraviolet
- a metal material is not very preferable because it reflects almost all electromagnetic waves.
- heat tolerance to process temperature in the film formation process and the heat treatment process performed according to need is also considered.
- a material of the separation layer 202 As a material of the separation layer 202, a material is used that causes , by being applied with an electromagnetic wave, reaction such as thermal decomposition or the like to generate a gas. Further, it desirably has heat tolerance to about 350 0 C or more in consideration of process temperature in the film formation process or the like. Specifically, similarly to those as explained in the first embodiment, a compound containing carbonate, sulfate or nitrate, or a metal compound such as metal nitride, metal sulfide ormetal carbide is used. The former decomposes to generate a gas by being applied with an electromagnetic wave having a predetermined wavelength. Further, the latter reacts with a component in an atmosphere or a material contained in an adjacent layer, i.e. , the substrate 201 or the layer to be peeled 203, which will be describe later, to generate a gas by being applied with an electromagnetic wave having a predetermined wavelength .
- the material of the layer to be peeled 203 is the same as that has explained in the first embodiment. Further, the method of fabricating the substrate 201 and the methods of forming the separation layer 202 and the layer to be peeled 203 are also the same as those have been explained in the first embodiment. Subsequently, heat treatment for improving the function of the function film may be performed on the structure for functional film pattern formation 201 to 203 according to need.
- a substrate for transfer 204 is prepared, and the structure for functional filmpattern formation 201 to 203 is provided and fixed such that the layer to be peeled 203 faces the substrate for transfer.
- the layer to be peeled 203 and the substrate for transfer may be fixed to each other by using an adhesive agent or the like.
- the substrate for transfer 204 a desired substrate such as a synthesized resin substrate of epoxy or the like or glass substrate may be used. Further, electrodes and interconnections may be formed at the substrate for transfer side in advance.
- an electromagnetic wave is applied to the structure for functional film pattern formation 201 to 203.
- reaction such as decomposition occurs in the separation layer 202 and a gas is generated.
- the layer tobepeeled203 is peeled from the substrate 201 and the layer to be peeled 203 is transferred to the substrate for transfer 204 as shown in Fig. 3C.
- the bonding strength between the layer to be peeled 203 and the substrate 201 becomes lower as a result of generating the gas, and thereby, the layer to be peeled 203 can be dynamically and easily peeled form the substrate 201.
- the layer to be peeled 203 can be transferred by peeling the substrate for transfer 204 at the same time as application of an electromagnetic wave or at the subsequent step.
- the electromagnetic wave an electromagnetic wave capable of causing the reaction such as deposition in the
- the microwave is an electromagnetic wave having a wavelength of about Im to lmm, and includes UHF wave (decimeter wave) , SHF wave (centimeter wave) , EHF wave (millimeter wave) and submillimeter wave .
- an infrared ray containing an absorption wavelength of the separation layer material is applied to the separation layer 202
- molecules contained in the separation layer material absorb infrared energy to greatly vibrate, and consequently, reaction such as decomposition occurs in the separation layer .
- an infrared ray having a wavelength of about 6.8 ⁇ m or ll. ⁇ m is applied to calcium carbonate is cited.
- an ultraviolet ray containing a component having the absorption wavelength of the separation layer material is applied to the separation layer 202
- atoms contained in the separation layermaterial absorb ultraviolet energy and outer electrons transition and become activated, and consequently, reaction such as decomposition occurs in the separation layer.
- an electromagnetic wave may be applied toward the side surface of the structure for functional film pattern formation .
- the separation layer202 generates heat and reaction occurs according to the principle of microwave heating.
- the absorption energy P of the microwave is expressed by the following equation (1) .
- ⁇ represents an electric conductivity
- f (Hz) represents a frequency of the microwave
- ⁇ o represents a dielectric constant of vacuum
- ⁇ r " represents a relative dielectric constant (complex)
- ⁇ 0 represents a permeability of vacuum
- ⁇ r " represents a relative permeability (complex)
- E represents an electric field intensity
- H represents a magnetic field intensity.
- the first term of the equation (1) represents joule loss (resistance loss)
- the second term represents dielectric loss
- the third item represents magnetic hysteresis loss .
- the electromagnetic wave absorbing layer 202 is rapidly and uniformly heated to the interior thereof by being applied withmicrowave . Accordingly, reaction such as decomposition is quickly caused in the separation layer 202, and the layer to be peeled 203 can be peeled from the substrate 201 in a short period of time, or the bonding strength of them can be reduced. Further, while the microwave is applied, only the region applied with the microwave is locally heated, and when the application of microwave is stopped, the region is rapidly cooled, and therefore, the influence on other layers
- the microwave can reach the interior of the functional film containing structure without especially limiting an orientation of the microwave to be applied to the functional film containing structure.
- a quartz mold is fabricated.
- a resist is applied to a quartz substrate, and exposure to light and development are performed, and thereby, a resist pattern is formed.
- a pattern is formed on the quartz substrate by dry etching by using the resist pattern as a mask. Furthermore, ashing (resist peeling) is performed.
- a tantalum nitride (TaN) film having a thickness of about 0. l ⁇ m is formed as a separation layer by using a PLD (pulse laser deposition) method.
- a lower electrode of platinum (Pt) is formed on the tantalum nitride film by using the sputtering method, and a BST (barium strontium titanate) film having a thickness of about 200nm is formed thereon by using the PLD method.
- the substrate temperature is heated to about 550 0 C .
- an upper electrode of platinum is formed on the BST film by using the sputtering method, and thereby, a Pt/BST/Pt thin film capacitor is fabricated.
- an adhesive agent is applied onto the upper electrode of the Pt/BST/Pt thin film capacitor formed on the projecting portions of the mold, and bonded to an epoxy substrate for transfer . Furthermore, whenaKrFexcimer laser beam (wavelength 248nm) is applied from the rear side of the mold toward the tantalum nitride film, the tantalum nitride film reacts and generates a gas . Thereby, the Pt/BST/Pt thin film capacitor is peeled from the mold and transferred to the substrate for transfer.
- the functional film can be easily peeled from the substrate or the bonding strength between them can be reduced for easy peeling at relatively low temperature (about 10 0 C to about 100 0 C) by applying an electromagnetic wave to the separation layer. Therefore, an element containing a functional film formed by using the film formation technology such as the evaporation method and the AD method through predetermined process temperature (e.g. , about 350 0 C or more) or a functional film provided with a high function by heat treatment at high temperature (e.g. , about 800 0 C) can be easily transferred to a desired substrate and utilized. That is, the transfer can be performed to a resin substrate having relatively lowheat tolerance, and therefore, the range of choices of substrates canbe expandedto a flexible substrate, for example, according to application.
- predetermined process temperature e.g. , about 350 0 C or more
- a functional film provided with a high function by heat treatment at high temperature e.g. , about 800 0 C
- an electromagnetic wave may be applied while heating the structure for functional film pattern formation.
- the reaction in the separation layer 202 can be promoted, and the layer to be peeled 203 can be peeled from the substrate 201 or the bonding strength between them can be reduced in a shorter time or with a weaker electromagnetic wave.
- the effect of improving the function of the functional film is expected by adjusting the heat treatment temperature according to the material of the functional film.
- an electromagnetic wave absorbing layer 210 is further formed between the substrate 201 and the separation layer 202.
- the electromagnetic wave absorbing layer 210 is a layer that absorbs, when an electromagnetic wave is applied, the
- electromagnetic energy thereof to generate heat is formed by carbon, ceramics, glass or the like .
- the material of the electromagnetic wave absorbing layer 210 is desirably determined according to an electromagnetic wave to be used in the subsequent step (an electricwave includingamicrowave, or an infraredray, etc . ) .
- Such a structure for functional film pattern formation is provided on the substrate for transfer 204, and the electromagnetic wave is applied toward the electromagnetic wave absorbing layer 210.
- the adjacent separation layer 202 is heatedby the electromagnetic wave absorbing layer 210 which is generating heat, reaction such as decomposition occurs in the separation layer 202, and a gas is generated.
- the layer to be peeled is provided on the substrate for transfer 204, and the electromagnetic wave is applied toward the electromagnetic wave absorbing layer 210.
- the layer to be peeled 203 is peeled from the substrate 201 and transferred to the substrate for transfer 204.
- the bonding strength between the layer to be peeled 203 and the substrate 201 or the electromagnetic wave absorbing layer 210 becomes lower as a result of generating the gas, and thereby, the layer to be peeled 203 can be transferred by peeling the substrate for transfer 204 at the same time as the application of an electromagnetic wave or at the subsequent step.
- the separation layer itself has little sensitivity to an electromagnetic wave, that is, its reactivity to an electromagnetic wave is not high, reaction because of heat canbe produced in the separation layer . Therefore, the range of choices of kinds (wavelengths) of electromagnetic waves and separation layer materials can be expanded.
- Figs . 5A to 5C are diagrams for explanation of the method of manufacturing a functional film according to the embodiment.
- the method of manufacturing a functional film according to the embodiment is characterizedin thataphysical andexternal force is used at the step (step S5) of peeling the layer to be peeled from the substrate.
- a structure for functional film pattern formation 301 to 303 including a substrate 301, a separation layer 302 , and a layer to be peeled 303 is fabricated (steps Sl to S3 in Fig. 1) , and a substrate for transfer 304 is provided and fixed (step S4 in Fig. 1) .
- a single crystal substrate including a semiconductor single crystal substrate and an oxide single crystal substrate, a ceramic substrate, a glass substrate or a metal substrate as those have been cited in the first embodiment may be used, and a material having heat tolerance to a process temperature in the film formation process when the functional film is formed and heat treatment process performed according to need is selected among them.
- a material that easily fractures by being applied with an external force As the material of the separation layer 302 , a material that easily fractures by being applied with an external force
- a material having cleavage characteristics is used. Further, in consideration of process temperature at the subsequent process (e.g. , about 350 0 C or more) , it is desired that a material having heat tolerance is used.
- a material having heat tolerance is used.
- hexagonal boron nitride (h-BN) mica, graphite, transitionmetal chalcogenide includingmolybdenumdisulfide
- the material of the layer to be peeled 303 is the same as that has explained in the first embodiment. Further, the method of fabricating the substrate 301 and the method of forming the layer to be peeled 303 are also the same as those have been explained in the first embodiment.
- the substrate for transfer 304 a substrate having a certain degree of elasticity such as a synthesized resin substrate of epoxy or the like is desirably used. Further, electrodes andinterconnectionsmaybe formedat the substrate for transfer 304 side in advance. Furthermore, the layer to be peeled 303 and the substrate for transfer 304 may be fixed using an adhesive agent or the like.
- an external force is applied to the separation layer 302.
- the substrate for transfer 304 may be relatively displaced or deformed to the separation layer 302.
- the substrate for transfer 304 may be peeled from the substrate 301, or the substrate for transfer 304 may be pulled in the' horizontal direction relative to the substrate 301.
- fracture is produced within the separation layer 302 or at an interface thereof, and the layer to be peeled 303 is peeled from the substrate 301 and transferred to the substrate for transfer 104 as shown in Fig.5C.
- the bonding strength between the layer to be peeled 303 and the substrate 301 becomes lower by applying an external force, and thereby, the layer to be peeled 303 may be transferred by further pulling up the substrate for transfer 304.
- a quartz mold is fabricated.
- a resist is applied to a quartz substrate, and a resistpattern is formed by performing exposure to light and development. Then, apattern is formedon the quartz substratebydryetching by using the resist pattern as a mask. Furthermore, ashing (resist peeling) is performed.
- a hexagonal boron nitride (h-BN) filmhaving a thickness of about 0.2 ⁇ m is formed as a separation layer by using a reactive sputtering method.
- a lower electrode of platinum (Pt) is formed on the hexagonal boron nitride film by using the sputtering method, and a BST
- the substrate is heated to a temperature of about 550 0 C.
- an upper electrode of platinum is formed on the BST film by using the sputtering method, and thereby, a Pt/BST/Pt thin film capacitor is fabricated.
- an adhesive agent is applied onto the upper electrode of the Pt/BST/Pt thin film capacitor formed on the projecting portions of the mold, and bonded to an epoxy substrate for transfer. Furthermore, when the mold is fixed andan external force is applied to the hexagonalboron nitride film by pulling up the substrate for transfer, fracture is produced in the film.
- the Pt/BST/Pt thin film capacitor is peeled from the mold and transferred to the substrate for transfer .
- the functional film can be easily peeled from the film formation substrate or the bonding strength between them can be reduced for easy peeling by applying an external force to the separation layer.
- temperature neverrises notonlyoutsideof the structure for functional filmpattern formationbutalso inside thereof, and the functional film and the element containing the functional film can be transferred to a resin substrate having relatively low heat tolerance and utilized.
- h-BN is stable in an oxygen atmosphere and has heat tolerance to about 800 0 C to 1000 0 C. Accordingly, in the case where a PZT film is fabricated by using h-BN as the separation layer, the piezoelectric property of the PZT film can be improved by performing heat treatment at about 800 0 C, for example.
- an external force may be applied to the separation layer 302 while heating the structure for functional filmpattern formation .
- fracture is easily produced in the separation layer 302, and the layer to be peeled 303 can be peeled with weaker force.
- improvement in the function of the functional film is expected by adjusting the heat treatment temperature according to the material of the functional film.
- the materials of the substrate for transfer 304 and adhesive agent are desirably selected according to the heat treatment temperature .
- an external force may be applied to the separation layer 302 while applying an electromagnetic wave to the structure for functional film pattern formation.
- the material contained in the separation layer 302 is activated by being applied with an ultraviolet ray and the separation layer 302 is heated by being applied with an infrared ray or a microwave, fracture can be produced in the separation layer 302 with weaker force .
- light such as an ultraviolet ray and an infrared ray
- At least one electrode may be formed on an upper surface or a lower surface of the functional film.
- a layer to be peeled 105 including an electrode layer 105a and a functional material layer 105b may be formed, or, as shown in Fig. 7, a layer to be peeled 106 including a functional material layer 106a and an electrode layer 106b may be formed.
- a layer to be peeled including electrode layers on both of upper and lower surfaces of the functional material layer may be used.
- the electrode layers 105a and 106b may be formed by using a known method such as a sputtering method and an evaporation method.
- the layer tobepeeled has been transferred to the substrate for transfer at the same time as beingpeeled from the substrate .
- the peeling of the layer to be peeled may be performed without using the substrate for transfer .
- a functional film molded in a desired shape in advance, or a functional element containing a functional film and an electrode can be obtained.
- an external force may be applied to the separation layer by applying physical stimulation (e.g., impact) to the side surface of the separation layer or the like.
- the substrate (101, 201, 301) to be used in the above-mentioned first to third embodiments can be reused by removing the residual separation layer by cleansing, etching or the like after peeling the layer to be peeled. Therefore, a number of the substrates can be suppressed and the cost of manufacture can be reduced.
- the present invention can be applied to memory elements, piezoelectric elements, pyroelectric elements, passive elements such as capacitors, optical elements, superconducting elements, photoelectric conversion elements , micromagneticelements andsemiconductorelements containing functional materials such as dielectric materials, piezoelectric materials , pyroelectric materials , magnetic material and semiconductor materials , and instruments to which those elements are applied.
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Abstract
A method of manufacturing a functional film which method enables formation of a fine pattern and endurance for a high-temperature process. The method includes the steps of: (a) preparing a substrate (101) in which a predetermined pattern is formed; (b) forming a separation layer (102, 202, 302) directly or indirectly on the substrate (101); (c) forming a layer to be peeled (103) containing a functional film (103), which is formed by using a functional material, on the separation layer (102); and (d) peeling the layer to be peeled (103) from the substrate (101) or reducing bonding strength between the layer to be peeled (103) and the substrate (101) by heating the separation layer (102), applying an electromagnetic wave toward the separation layer (202), or applying an external force to the separation layer (302).
Description
DESCRIPTION
STRUCTURE FOR FUNCTIONAL FILM PATTERN FORMATION AND
METHOD OF MANUFACTURING FUNCTIONAL FILM
TECHNICAL FIELD
The present: invention relates to a method of manufacturing a functional film including a dielectric material, piezoelectric material, pyroelectric material, magnetic material, semiconductor material or the like, and specifically to amethod of manufacturing the functional film having a pattern . Further, the present invention relates to a structure for functional film pattern formation to be used in a manufacturing process of the functional film.
BACKGROUND ART
Recent years, in response to the needs for electronic devices such as miniaturization, speeding up, integration, andmultifunctionality, themanufactureofdevices containing functional materials such as electronic ceramics, which express predetermined functions by being applied with electric fields or magnetic fields and include a dielectric material, piezoelectric material, magnetic material, pyroelectric material and semiconductor material, by using various film formation technologies has been actively studied.
For example, in order to enable high-definition and
high-quality printing in an inkjet printer, it is necessary to miniaturize and highly integrate ink nozzles of inkjet heads. Accordingly, it is also necessary to similarly miniaturize andhighly integrate piezoelectric actuators for driving the respective ink nozzles. In such a case, a film formation technology, that enables formation of a thinner layer than a bulk material and formation of fine patterns, is desired, and film formation technologies such as a sputteringmethod, a sol-gelmethod, andan aerosol deposition method have been studied.
Conventionally, photolithography has been used for patterning a filmof functionalmaterial (also simply referred to as "functional film") . That is, schematically, a functional film layer is formed on a substrate, a mask pattern is formed by applying a resist onto the film and performing exposure to light and development thereon, and further, the functional film layer is dry etchedor wet etched, and thereby, a functional film pattern is obtained.
However, it is known that the functional film formed by film formation does not sufficiently exert its function in a condition after the film formation, and the film is inferior to a bulk material in performance . Accordingly, in order to sufficiently express the function of a functional film, heat treatment at relatively high temperature (e.g., about 5000C to 10000C) is required after film formation.
Further, since a film formation substrate is simultaneously heat-treated when the heat treatment is performed on the
functional film, high heat tolerance is required for the material of film formation substrate. On the other hand, in the case where a fabricated function film is utilized, there is demand for using various kinds of substrates according to instruments such as a flexibly substrate made of resin, for example . Accordingly, a method has been studiedby which a functional film formed on a film formation substrate can be peeled or transferred from the film formation substrate without hindering its function. As a related technology, Japanese Patent Application Publication JP-P2005-64289A discloses a method for forming a high-density micropattern. The method includes the steps of forming an organicmonomolecular film on a first substrate, microfabricating the organic monomolecular film by photolithography to form an organic monomolecular film pattern, selectively growing a thin film on the organic monomolecular film pattern, and transferring the thin film onto a second substrate to form a micropattern of the thin film on the second substrate (page 2) . According to the method disclosed in JP-P2005-64289A, the patterned functional film (the thin film 15 shown in Fig. 4 of JP-P2005-64289A) can be transferred relatively easily. However, the organicmonomolecular filmis usedin thismethod, and therefore, it is impossible to form the functional film by a high-temperature process nor perform high-temperature heat treatment on the formed functional film.
DISCLOSURE OF THE INVENTION
Accordingly, in view of the above-mentioned problems , a firstpurpose of the present invention is to provide amethod of manufacturing a functional film by which a fine pattern can be formed. Further, a second purpose of the present invention is to provide amethod ofmanufacturing a functional film by which a functional film formed through a high temperature process can be provided on a desired substrate. Furthermore, a third purpose of the present invention is to provide a structure for functional film pattern formation to be used in a manufacturing process of such a functional film.
In order to accomplish the purposes, a structure for functional film pattern formation according to one aspect of the present invention includes : a substrate in which a predetermined pattern is formed; a separation layer directly or indirectly provided on the substrate; and a layer to be peeled provided on the separation layer and containing a functional filmformedbyusing a functionalmaterial , wherein the layer to be peeled is peeled from the substrate or bonding strength between the layer to be peeled and the substrate becomes lower by heating the separation layer, applying an electromagnetic wave toward the separation layer, or applying an external force to the separation layer. A method of manufacturing a function film according to one aspect of the present invention includes the steps of: (a) preparing a substrate in which a predetermined pattern
is formed; (b) forming a separation layer directly or indirectly on the substrate; (c) forming a layer to be peeled containing a functional film, which is formed by using a functional material , on the separation layer; and (d) peeling the layer to be peeled from the substrate or reducing bonding strength between the layer to be peeled and the substrate by heating the separation layer, applying an electromagnetic wave toward the separation layer, or applying an external force to the separation layer. Here, "reaction" refers to a process in which, from one material or material system, another material or material system different from the initial material or material system in composition or structure is produced. And "reaction" includes a process in which one kind of compound changes into two or more kinds of simplermaterials , and a process in which, based on two kinds of materials including at least one kind of compound, two or more kinds of materials different from the initial materials are produced. Further, the former case is specifically referred to as "decomposition" , and the decomposition brought about by heating is referred to as "thermal decomposition" .
According to the present invention, the functional film is formed on the substrate in which the pattern has been formed in advance, and thereby, the process of performing dry etching orwetetchingon the functional film canbe omitted. Although sometimesdamageis causedtothefunctionalfilmintheetching step depending on the material, such damage is not caused
according to the present invention . Further, the functional film is formed on the substrate via the separation layer, and therefore, by applying heat, an electromagnetic wave or an external force to the layer to be peeled, the substrate and the functional film can be easily peeled, or the bonding strength between them is reduced such that they can be dynamically and easily peeled at the subsequent step. Accordingly, the fine functional film pattern formed through the high temperature process can be easily transferred to a flexible substrate, for example, having relatively low heat tolerance and utilized. Therefore, elements having advantageous properties can be suitably mounted on instruments according to application and the performance of the entire instruments utilizing such elements can be improved.
BRIEF DESCRIPTION OF THE DRAWINGS
Advantages and features of the present invention will be apparentby considering the following detaileddescription and the drawings in relation. In these drawings, the same reference numerals indicate the same component elements .
Fig. 1 is a flowchart showing a method of manufacturing a functional film according to the first to third embodiments of the present invention. Figs . 2A to 2F are sectional views for explanation of the method of manufacturing a functional film according to • the first embodiment of the present invention.
Figs. 3A to 3C are sectional views for explanation of the method of manufacturing a functional film according to the second embodiment of the present invention.
Figs . 4A and 4B are sectional views for explanation of amodified example of the method of manufacturing a functional film according to the second embodiment of the present invention.
Figs . 5A to 5C are sectional views for explanation of the method of manufacturing a functional film according to the third embodiment of the present invention.
Fig. 6 is a sectional view showing a modified example of a structure for functional film pattern formation.
Fig. 7 is a sectional view showing another modified example of the structure for functional film pattern formation.
BEST MODE FOR CARRYING OUT THE INVENTION
Fig. 1 is a flowchart showing a method of manufacturing a functional film according to the first to third embodiments of thepresent invention . Further, Figs .2Ato 2Fare diagrams for explanation of the method of manufacturing a functional filmaccordingto the firstembodimentof thepresentinvention in which Figs . 2A to 2C show steps of fabricating a structure for functional film pattern formation according to the first embodiment of the present invention.
First, at step Sl in Fig. 1, a substrate (mold) 101, inwhichapatternhavingprojections anddepressions is formed,
is prepared as shown in Fig. 2A. In the substrate, the projecting portions correspond to a pattern to be formed in a functional film as a target of manufacturing.
As a material of the substrate 101, a single crystal material including a semiconductor single crystal material and an oxide single crystal material, a ceramics material, a glass material, or a metal material may be used. The substrate material is selected in consideration of heat tolerance or the like to a process temperature in the film formation process when the functional film is formed and the heat treatment process performed according to need.
As an oxide single crystal material, specifically, magnesium oxide (MgO) , alumina (Al2O3) , titanium oxide (TiO2) , zinc oxide (ZnO) , spinel (magnesium aluminate, MgAl2O4) , strontium titanate (SrTiO3) , lanthanum aluminate (LaAlOs) , lithium niobate (LiNbO3) , lithium tantalate (LiTaO3) and so on are cited. In the case where the oxide single crystal material is used, by selecting a material having a predetermined lattice constant according to a functional film as a target ofmanufacturing, the functional filmcanbe formed by epitaxial growth. Further, since these materials are stable in an oxidizing atmosphere, they can be used for film formation or heat-treated at high temperature (e.g., about 10000C for magnesium oxide) in the air atmosphere. As a semiconductor single crystalmaterial, specifically, silicon (Si) , germanium (Ge) , gallium arsenide (GaAs) ,
- gallium phosphide (GaP) , indium phosphide (InP) and so on
are cited. In the case where the semiconductor single crystal material is used, by selecting a material having a predetermined lattice constant according to a functional film as a target ofmanufacturing, the functional filmcanbe formed by epitaxial growth. Further, since these materials are stable in a reducing atmosphere, they can be used for film formation or heat-treated at high temperature (e.g. , about 10000C for silicon) in the reducing atmosphere.
As a ceramicsmaterial , alumina (Al2O3) , zirconia (ZrO2) , aluminumnitride (AlN) andso on are cited. Since the ceramics material is more inexpensive than the single crystalmaterial , thecostofmanufacturingcanbereduced. Further, sincethese materials are stable in the air atmosphere and have high heat tolerance, they canbe used for film formation or heat-treated at high temperature (e.g., about 11000C for alumina) in the air atmosphere.
As a glass material, specifically, silicate glass, alkaline silicateglass, borosilicateglass , soda-limeglass , lead glass and so on are cited. Since the glass material is more inexpensive than the single crystal material, the cost of manufacturing can be reduced. Further, since these materials are stable in an oxidizing atmosphere, they can be used for film formation or heat-treated at high temperature
(e.g. , about 9000C for silicate glass) in the air atmosphere. As ametalmaterial, specifically, metal such asplatinum
(Pt) , copper (Cu) , nickel (Ni) , iron (Fe) and so on, and alloy such as stainless steel are cited. Since the metal material
is more inexpensive than the single crystal material, the cost of manufacturing can be reduced. Further, since these materials are stable in a reducing atmosphere, they can be used for film formation or heat-treated at high temperature (e.g. , about 10000C for platinum) in the reducing atmosphere.
The substrate 101 can be fabricated by forming a pattern in a substrate made of the above-mentioned material by using dry etching, electron beam lithography or the like. In this regard, for example, a mold fabrication technology used in nanoimprint technology may be applied. Alternatively, a commercially available nanoimprint mold may be used.
Next, at step S2 , a separation layer 102 is formed on the substrate 101, as shown in Fig.2B. The separation layer 102 is a sacrifice layer that is removed when a functional film to be formed at the subsequent step is peeled from the substrate 101. As a material of the separation layer 102, a material that induces a reaction of thermal decomposition or the like by being heated to generate a gas is used. Specifically, a compoundcontainingat least one of carbonates of magnesium carbonate (MgCO3, decomposed at about 6000C) , calcium carbonate (CaCO3, decomposed at about 9000C) , strontiumcarbonate (SrCO3, decomposedat about 9000C) , barium carbonate (BaCO3, decomposed at about 14500C) , lithium carbonate (LiCO3, decomposedatabout 618°C) , sodiumcarbonate (Na2CO3) , potassium carbonate (K2CO3) and so on, a compound containing at least one of sulfates ofmagnesium sulfate (MgSO4, • decomposed at about 1185°C) , calcium sulfate (CaSO4,
decomposed at about 10000C) , strontium sulfate (SrSO4, decomposedatabout 11300C) , barium sulfate (BaSO4, decomposed at about 12000C) , ferrous sulfate (FeSO4) , cobalt sulfate (CoSO4) , nickel sulfate (NiSO4) , zinc sulfate (ZnSO4) , lead sulfate (PbSO4), bismuth sulfate (Bi (SO4) 3) and so on, and a compound containing at least one of nitrates of strontium nitrate (Sr(NO3J2), cesium nitrate (CsNO3) and so on are used. These compounds are decomposed by being applied with an electromagnetic wave having a predetermined wavelength to generate gases. For example, by heating calcium carbonate, decomposition reaction (CaCO3 —> CaO + CO2T) occurs and carbon dioxide (CO2) is generated.
Alternatively, metal nitride containing at least one element of Ti, V, Cr, Mh, Fe, Co, Ni, Ga (gallium nitride is decomposed at about 9000C) , Zr, Mo (molybdenum nitride is decomposed at about 9000C) , Ta andW, metal sulfide containing at least one element of V, Cr, Mn, Fe, Co, Ni, Mo, Ta and W, andmetal carbide such as TiC may be used. These compounds are applied with an electromagnetic wave having a predetermined wavelength to react with components in the atmosphere or an adjacent layer, i.e. , components contained in the substrate 101 or a layer to be peeled 103, which will be described later, to generate a gas. For example, in the case where a substrate containing oxide and a separation layer containingmetal nitride areused, the separation layer reacts with the oxide to generate nitrogen (N2) .
As a method of forming the separation layer, a known
method such as spin coating, sputtering and CVD (chemical vapor deposition) methods may be used.
Next, at step S3, a layer to be peeled 103 containing a material of a functional film as a target of manufacturing (functional material) is formed on the separation layer 102, as shown in Fig. 2C. The layer to be peeled 103 is formed by using a known method such as a sputtering method, a CVD method, a sol-gelmethodandanaerosol deposition (AD) method. Here, the AD method is a film forming method of generating an aerosol in which raw material powder is dispersed in a gas, injecting the aerosol from a nozzle toward a substrate to allow the raw material powder to collide with the under layer, and thereby, depositing the raw material on the substrate, andthemethodis also called "injection deposition method" or "gas deposition method" .
In theembodiment, specifically, the followingmaterials are used as functional materials .
As a material of a functional film to be used for a memory element, Pb (Zr,Ti) O3, SrBi2 (Ta,Nb)2O9, Bi4Ti3Oi2 and so on are cited.
As a material of a functional film to be used for a piezoelectric element such as an actuator, Pb (Zr,Ti) O3, Pb(Mgi/3Nb2/3)O3, Pb(Zni/3 Nb2/3)O3, Pb (Nii/3 Nb2/3)O3 and so on, and solid solutions thereof are cited. As a material of a functional film to be used for a pyroelectric element such as an infrared sensor, Pb (Zr,Ti) O3, (Pb,La) (Zr,Ti) O3 and so on are cited1.
As amaterial of a functional film to be used for apassive component such as a capacitor, BaSrTiO3, (Pb,La) (Zr7Ti)O3 and so on are cited.
As a material of a functional film to be used for an optical element such as an optical switch, (Pb,La) (Zr,Ti) O3, LiHbO3 and so on are cited.
As a material of a functional film to be used for a superconducting element such as a superconducting quantum interference device (SQUID) , YBa2Cu3O7, Bi2Sr2Ca2Cu3Oi0 and so on are cited. Here, SQUID refers to a highly sensitive magnetic sensor element utilizing superconductivity.
As a material of a functional film to be used for a photoelectric conversion element such as a solar cell, amorphous silicon and compound semiconductor are cited. As a material of a functional film to be used for a micro magnetic element such as a magnetic head, PdPtMn, CoPtCr and so on are cited.
As a material of a functional film to be used for a semiconductor element such as a TFT, amorphous silicon and so on are cited.
The structure for functional film pattern formation according to the embodiment includes the substrate 101, the separation layer 102 and the layer to be peeled 103 formed at those steps Sl to S3. Next, at step S4 , a substrate for transfer104 isprepared, and the structure for functional film pattern formation 101 to 103 is provided and fixed such that'the layer to be peeled
103 faces the substrate for transfer 104, as shown in Fig. 2D . Inthisregard, thelayertobepeeled.103 andthe substrate for transfer 104 maybe fixed to each otherby using an adhesive agentor the like . As the substrate for transfer 104 , adesired substrate such as a synthesized resin substrate of epoxy or the like or glass substrate may be used. Further, electrodes and interconnections may be formed at the substrate for transfer 104 side in advance.
Next, at step S5, heat treatment is performed on the structure for functional film pattern formation 101 to 103. The temperature of the heat treatment is set to the same level with the reaction temperature of the separation layer 102 or more in order to cause the reaction such as thermal composition or the like in the separation layer 102. Thereby, as shown in Fig. 2Ξ, reaction such as thermal decomposition occurs in the separation layer 102 and a gas is generated. As a result, as shown in Fig. 2F, the layer to be peeled 103 is peeled from the substrate 101 and transferred to the substrate for transfer 104. Alternatively, the bonding strength between the layer to be peeled 103 and the substrate 101 becomes lower as a result ofgenerating the gas , andthereby, the layer to bepeeled 103 canbe dynamically and easilypeeled form the substrate 101. In this case, the layer to be peeled 103 can be transferred by peeling the substrate for transfer 104 at the same time as heating or at the subsequent step.
Further, at step S5, heat treatment (post anneal) for
■ promoting grain growth in the functional film or improving
crystallinity to improve the function of the film may be performed. For example, in the case of manufacturing a functional film of Pb (Zr,Ti) O3, (Pb,La) (Zr,Ti) O3, BaSrTi3 or the like, heat treatment is performed at temperature of 5000C or more . Further, in the case of manufacturing a functional film of SrBi2 (Ta,Nb)2O9, Bi4Ti3Oi2, YBa2Cu3O7, Bi2Sr2Ca2Cu3Oi0Or the like, heat treatment is performed at temperature of 7000C ormore . In this case, it is necessary to select thematerials of the substrate for transfer 104 and adhesive agent in consideration of heat tolerance to the heat treatment temperature .
As described above, according to the first embodiment of the present invention, since the separation layer is provided between the substrate and the functional film, the functional film can be peeled from the substrate by heat treatment or they can be made easier to be peeled by reducing the bonding strength between them. Accordingly, a high-performance functional film fabricated by a film formation technology can be provided in a desired pattern on a desired substrate. Further, since the heat treatment process and the peeling (transfer) process can be performed at the same timeby selecting the appropriate separation layer material according to the heat treatment temperature and heat treatment atmosphere for the functional film, the manufacturing process becomes simpler and the cost of manufacturing can be reduced.
Next, a method of manufacturing a functional film
according to the second embodiment will be explained by referring to Figs .1 and 3A to 3C . Figs .3A to 3C are sectional views for explanation of the method of manufacturing a functional film according to the embodiment. The method of manufacturing a functional film according to the embodiment is characterized in that an electromagnetic wave is used at the step (S5) of peeling the layer to be peeled from the substrate .
First, at steps Sl to S3 of Fig. 1, a structure for functional film pattern formation 201 to 203 including a substrate 201 , a separation layer 202 and a layer to be peeled 203 is fabricated, as shown in Fig. 3A.
As the material of the substrate 201, suitable one is selected from a single crystal material including a semiconductor single crystal material and an oxide single crystal material, a ceramics material and a glass material according to a wavelength of the electromagnetic wave to be used and so on . For example, in the case where light such as ultraviolet is used at step S5, it is desired to use a substrate through which a predeterminedwavelength component is propagated or transmitted. Unlike the first embodiment, a metal material is not very preferable because it reflects almost all electromagnetic waves. Further, it is desirable that heat tolerance to process temperature in the film formation process and the heat treatment process performed according to need is also considered.
As a material of the separation layer 202, a material
is used that causes , by being applied with an electromagnetic wave, reaction such as thermal decomposition or the like to generate a gas. Further, it desirably has heat tolerance to about 3500C or more in consideration of process temperature in the film formation process or the like. Specifically, similarly to those as explained in the first embodiment, a compound containing carbonate, sulfate or nitrate, or a metal compound such as metal nitride, metal sulfide ormetal carbide is used. The former decomposes to generate a gas by being applied with an electromagnetic wave having a predetermined wavelength. Further, the latter reacts with a component in an atmosphere or a material contained in an adjacent layer, i.e. , the substrate 201 or the layer to be peeled 203, which will be describe later, to generate a gas by being applied with an electromagnetic wave having a predetermined wavelength .
The material of the layer to be peeled 203 is the same as that has explained in the first embodiment. Further, the method of fabricating the substrate 201 and the methods of forming the separation layer 202 and the layer to be peeled 203 are also the same as those have been explained in the first embodiment. Subsequently, heat treatment for improving the function of the function film may be performed on the structure for functional film pattern formation 201 to 203 according to need.
Next, at step S4 in Fig. 1, a substrate for transfer 204 is prepared, and the structure for functional filmpattern
formation 201 to 203 is provided and fixed such that the layer to be peeled 203 faces the substrate for transfer. In this regard, the layer to be peeled 203 and the substrate for transfer may be fixed to each other by using an adhesive agent or the like. As the substrate for transfer 204, a desired substrate such as a synthesized resin substrate of epoxy or the like or glass substrate may be used. Further, electrodes and interconnections may be formed at the substrate for transfer side in advance. Next, at step S5, an electromagnetic wave is applied to the structure for functional film pattern formation 201 to 203. Thereby, as shown in Fig. 3B, reaction such as decomposition occurs in the separation layer 202 and a gas is generated. As a result, the layer tobepeeled203 is peeled from the substrate 201 and the layer to be peeled 203 is transferred to the substrate for transfer 204 as shown in Fig. 3C. Alternatively, the bonding strength between the layer to be peeled 203 and the substrate 201 becomes lower as a result of generating the gas, and thereby, the layer to be peeled 203 can be dynamically and easily peeled form the substrate 201. In this case, the layer to be peeled 203 can be transferred by peeling the substrate for transfer 204 at the same time as application of an electromagnetic wave or at the subsequent step. As the electromagnetic wave, an electromagnetic wave capable of causing the reaction such as deposition in the
' separation layer 202 is selectedamongamicrowave, an infrared
ray, a visible ray, an ultraviolet ray and an X-ray. Here, the microwave is an electromagnetic wave having a wavelength of about Im to lmm, and includes UHF wave (decimeter wave) , SHF wave (centimeter wave) , EHF wave (millimeter wave) and submillimeter wave .
For example, in the case where an infrared ray containing an absorption wavelength of the separation layer material is applied to the separation layer 202, molecules contained in the separation layer material absorb infrared energy to greatly vibrate, and consequently, reaction such as decomposition occurs in the separation layer . Specifically, the case where an infrared ray having a wavelength of about 6.8μm or ll.βμm is applied to calcium carbonate is cited. Further, in the case where an ultraviolet ray containing a component having the absorption wavelength of the separation layer material is applied to the separation layer 202 , atoms contained in the separation layermaterial absorb ultraviolet energy and outer electrons transition and become activated, and consequently, reaction such as decomposition occurs in the separation layer. Specifically, the case where an ultraviolet ray having a wavelength of about 248nm is applied to calcium carbonate is cited. In this case, there is an advantage that the substrate 201 and the layer to be peeled 203 are not affected by heat. In the case where light such as an infrared or ultraviolet ray is used, it is desired that the electromagnetic wave is applied from the substrate 201
' side toward the separation layer 202 as shown in Fig. 3B.
Alternatively, an electromagnetic wave may be applied toward the side surface of the structure for functional film pattern formation .
By the way, in the case where a microwave is applied to the separation layer 202 , the separation layer202 generates heat and reaction occurs according to the principle of microwave heating. Here, the absorption energy P of the microwave is expressed by the following equation (1) . P = (l/2)σ|E|2 + πfε0εr"|E|2 + πfμoμr"lH|2 ...(1) In equation (1) , σ represents an electric conductivity, f (Hz) represents a frequency of the microwave, εo represents a dielectric constant of vacuum, εr" represents a relative dielectric constant (complex) , μ0 represents a permeability of vacuum, μr" represents a relative permeability (complex) , E represents an electric field intensity, and H represents a magnetic field intensity. Further, the first term of the equation (1) represents joule loss (resistance loss) , the second term represents dielectric loss, and the third item represents magnetic hysteresis loss . When an electromagnetic field is applied by applying a microwave to the separation layer 102 , heat corresponding to energy expressed by the equation (1) is generated. As a result, reaction such as decomposition occurs in the separation layer 102. Therefore, in the case of using a microwave, inorder to efficientlygenerateheat, itis desired that a material having a large relative dielectric constant (complex) εr" , amaterial having a large1relative permeability
(complex) μr" , or a material having a large electric conductivity σ is used as the separation layer 102.
According to the principle of microwave heating, the electromagnetic wave absorbing layer 202 is rapidly and uniformly heated to the interior thereof by being applied withmicrowave . Accordingly, reaction such as decomposition is quickly caused in the separation layer 202, and the layer to be peeled 203 can be peeled from the substrate 201 in a short period of time, or the bonding strength of them can be reduced. Further, while the microwave is applied, only the region applied with the microwave is locally heated, and when the application of microwave is stopped, the region is rapidly cooled, and therefore, the influence on other layers
(e.g. , the layer tobepeeled203 andthe substrate for transfer 204) can be minimized. In the case of using a microwave, the microwave can reach the interior of the functional film containing structure without especially limiting an orientation of the microwave to be applied to the functional film containing structure. (Example 1)
First, a quartz mold is fabricated. For the purpose, a resist is applied to a quartz substrate, and exposure to light and development are performed, and thereby, a resist pattern is formed. Then, a pattern is formed on the quartz substrate by dry etching by using the resist pattern as a mask. Furthermore, ashing (resist peeling) is performed.
On the thus fabricated quartz mold, a tantalum nitride
(TaN) film having a thickness of about 0. lμm is formed as a separation layer by using a PLD (pulse laser deposition) method. A lower electrode of platinum (Pt) is formed on the tantalum nitride film by using the sputtering method, and a BST (barium strontium titanate) film having a thickness of about 200nm is formed thereon by using the PLD method. At this time, the substrate temperature is heated to about 5500C . Furthermore, an upper electrode of platinum is formed on the BST film by using the sputtering method, and thereby, a Pt/BST/Pt thin film capacitor is fabricated.
Then, an adhesive agent is applied onto the upper electrode of the Pt/BST/Pt thin film capacitor formed on the projecting portions of the mold, and bonded to an epoxy substrate for transfer . Furthermore, whenaKrFexcimer laser beam (wavelength 248nm) is applied from the rear side of the mold toward the tantalum nitride film, the tantalum nitride film reacts and generates a gas . Thereby, the Pt/BST/Pt thin film capacitor is peeled from the mold and transferred to the substrate for transfer. As described above, according to the second embodiment of the present invention, the functional film can be easily peeled from the substrate or the bonding strength between them can be reduced for easy peeling at relatively low temperature (about 100C to about 1000C) by applying an electromagnetic wave to the separation layer. Therefore, an element containing a functional film formed by using the film formation technology such as the evaporation method and the
AD method through predetermined process temperature (e.g. , about 3500C or more) or a functional film provided with a high function by heat treatment at high temperature (e.g. , about 8000C) can be easily transferred to a desired substrate and utilized. That is, the transfer can be performed to a resin substrate having relatively lowheat tolerance, and therefore, the range of choices of substrates canbe expandedto a flexible substrate, for example, according to application.
In the embodiment, at the transfer step (step S5 in Fig. 1) , an electromagnetic wave may be applied while heating the structure for functional film pattern formation. Thereby, the reaction in the separation layer 202 can be promoted, and the layer to be peeled 203 can be peeled from the substrate 201 or the bonding strength between them can be reduced in a shorter time or with a weaker electromagnetic wave. In addition, the effect of improving the function of the functional film is expected by adjusting the heat treatment temperature according to the material of the functional film.
Next, a modified example of the method of manufacturing a functional film according to the second embodiment of the present invention will be explained.
In the modified example, as shown in Fig. 4A, an electromagnetic wave absorbing layer 210 is further formed between the substrate 201 and the separation layer 202. The electromagnetic wave absorbing layer 210 is a layer that absorbs, when an electromagnetic wave is applied, the
" electromagnetic energy thereof to generate heat.
Specifically, it is formed by carbon, ceramics, glass or the like . The material of the electromagnetic wave absorbing layer 210 is desirably determined according to an electromagnetic wave to be used in the subsequent step (an electricwave includingamicrowave, or an infraredray, etc . ) .
Such a structure for functional film pattern formation is provided on the substrate for transfer 204, and the electromagnetic wave is applied toward the electromagnetic wave absorbing layer 210. Thereby, as shown in Fig. 4B, the adjacent separation layer 202 is heatedby the electromagnetic wave absorbing layer 210 which is generating heat, reaction such as decomposition occurs in the separation layer 202, and a gas is generated. As a result, the layer to be peeled
203 is peeled from the substrate 201 and transferred to the substrate for transfer 204. Alternatively, the bonding strength between the layer to be peeled 203 and the substrate 201 or the electromagnetic wave absorbing layer 210 becomes lower as a result of generating the gas, and thereby, the layer to be peeled 203 can be transferred by peeling the substrate for transfer 204 at the same time as the application of an electromagnetic wave or at the subsequent step.
According to themodified example, even in the case where the separation layer itself has little sensitivity to an electromagnetic wave, that is, its reactivity to an electromagnetic wave is not high, reaction because of heat canbe produced in the separation layer . Therefore, the range of choices of kinds (wavelengths) of electromagnetic waves
and separation layer materials can be expanded.
Next, a method of manufacturing a functional film according to the third embodiment of the present invention will be explained by referring to Figs .1 and 5A to 5C . Figs . 5A to 5C are diagrams for explanation of the method of manufacturing a functional film according to the embodiment. The method of manufacturing a functional film according to the embodimentis characterizedin thataphysical andexternal force is used at the step (step S5) of peeling the layer to be peeled from the substrate.
First, as shown in Fig. 5A, a structure for functional film pattern formation 301 to 303 including a substrate 301, a separation layer 302 , and a layer to be peeled 303 is fabricated (steps Sl to S3 in Fig. 1) , and a substrate for transfer 304 is provided and fixed (step S4 in Fig. 1) .
As the material of the substrate 301, a single crystal substrate including a semiconductor single crystal substrate and an oxide single crystal substrate, a ceramic substrate, a glass substrate or a metal substrate as those have been cited in the first embodiment may be used, and a material having heat tolerance to a process temperature in the film formation process when the functional film is formed and heat treatment process performed according to need is selected among them. As the material of the separation layer 302 , a material that easily fractures by being applied with an external force
' like a material having cleavage characteristics is used.
Further, in consideration of process temperature at the subsequent process (e.g. , about 3500C or more) , it is desired that a material having heat tolerance is used. As such a material, hexagonal boron nitride (h-BN) , mica, graphite, transitionmetal chalcogenide includingmolybdenumdisulfide
(MoS2) and so on are cited. Further, as a method of forming the separation layer 302, a known method such as sputtering and CVD (chemical vapor deposition) methods may be used.
The material of the layer to be peeled 303 is the same as that has explained in the first embodiment. Further, the method of fabricating the substrate 301 and the method of forming the layer to be peeled 303 are also the same as those have been explained in the first embodiment.
As the substrate for transfer 304, a substrate having a certain degree of elasticity such as a synthesized resin substrate of epoxy or the like is desirably used. Further, electrodes andinterconnectionsmaybe formedat the substrate for transfer 304 side in advance. Furthermore, the layer to be peeled 303 and the substrate for transfer 304 may be fixed using an adhesive agent or the like.
Next, at step S5, an external force is applied to the separation layer 302. As a method of applying an external force, the substrate for transfer 304 may be relatively displaced or deformed to the separation layer 302. Specifically, as shown in Fig.5B, the substrate for transfer 304 may be peeled from the substrate 301, or the substrate for transfer 304 may be pulled in the' horizontal direction
relative to the substrate 301. Thereby, fracture is produced within the separation layer 302 or at an interface thereof, and the layer to be peeled 303 is peeled from the substrate 301 and transferred to the substrate for transfer 104 as shown in Fig.5C. Alternatively, the bonding strength between the layer to be peeled 303 and the substrate 301 becomes lower by applying an external force, and thereby, the layer to be peeled 303 may be transferred by further pulling up the substrate for transfer 304. (Example 2)
First, a quartz mold is fabricated. For the purpose, a resist is applied to a quartz substrate, and a resistpattern is formed by performing exposure to light and development. Then, apattern is formedon the quartz substratebydryetching by using the resist pattern as a mask. Furthermore, ashing (resist peeling) is performed.
On the thus fabricated quartz mold, a hexagonal boron nitride (h-BN) filmhaving a thickness of about 0.2μm is formed as a separation layer by using a reactive sputtering method. A lower electrode of platinum (Pt) is formed on the hexagonal boron nitride film by using the sputtering method, and a BST
(barium strontium titanate) film having a thickness of about
200nm is formed thereonbyusing the PLDmethod. At this time, the substrate is heated to a temperature of about 5500C. Furthermore, an upper electrode of platinum is formed on the BST film by using the sputtering method, and thereby, a Pt/BST/Pt thin film capacitor is fabricated.
Then, an adhesive agent is applied onto the upper electrode of the Pt/BST/Pt thin film capacitor formed on the projecting portions of the mold, and bonded to an epoxy substrate for transfer. Furthermore, when the mold is fixed andan external force is applied to the hexagonalboron nitride film by pulling up the substrate for transfer, fracture is produced in the film. Thereby, the Pt/BST/Pt thin film capacitor is peeled from the mold and transferred to the substrate for transfer . As described above, according to the third embodiment of the present invention, the functional film can be easily peeled from the film formation substrate or the bonding strength between them can be reduced for easy peeling by applying an external force to the separation layer. At that time, temperature neverrises notonlyoutsideof the structure for functional filmpattern formationbutalso inside thereof, and the functional film and the element containing the functional film can be transferred to a resin substrate having relatively low heat tolerance and utilized. Further, since the material of the separation layer 302 tobeusedin theembodimenthas relativelyhighheattolerance, heat treatment can be performed on the functional film at ahigh temperaturebefore the layer tobepeeled304 isprovided. For example, h-BN is stable in an oxygen atmosphere and has heat tolerance to about 8000C to 10000C. Accordingly, in the case where a PZT film is fabricated by using h-BN as the separation layer, the piezoelectric property of the PZT film
can be improved by performing heat treatment at about 8000C, for example.
As a modified example of the method of manufacturing a functional film according to the embodiment, an external force may be applied to the separation layer 302 while heating the structure for functional filmpattern formation . Thereby, fracture is easily produced in the separation layer 302, and the layer to be peeled 303 can be peeled with weaker force. In this regard, improvement in the function of the functional film is expected by adjusting the heat treatment temperature according to the material of the functional film. In this case, the materials of the substrate for transfer 304 and adhesive agent are desirably selected according to the heat treatment temperature . Alternatively, as anothermodifiedexample of themethod ofmanufacturinga functional filmaccording to the embodiment, an external force may be applied to the separation layer 302 while applying an electromagnetic wave to the structure for functional film pattern formation. For example, since the material contained in the separation layer 302 is activated by being applied with an ultraviolet ray and the separation layer 302 is heated by being applied with an infrared ray or a microwave, fracture can be produced in the separation layer 302 with weaker force . In the case of applying light such as an ultraviolet ray and an infrared ray, it is desired to use a substrate material that is transparent to the electromagnetic wave to be used and the electromagnetic wave
is applied from the rear side of the substrate 301 toward the separation layer 302.
As a modified example of the structure for functional filmpattern formation to be used in the manufacturingprocess of the functional film according to the first to third embodiments of the present invention, at least one electrode may be formed on an upper surface or a lower surface of the functional film. For example, as shown in Fig. 6, a layer to be peeled 105 including an electrode layer 105a and a functional material layer 105b may be formed, or, as shown in Fig. 7, a layer to be peeled 106 including a functional material layer 106a and an electrode layer 106b may be formed. Further, a layer to be peeled including electrode layers on both of upper and lower surfaces of the functional material layer may be used. The electrode layers 105a and 106b may be formed by using a known method such as a sputtering method and an evaporation method.
Further, in the first to third embodiments, the layer tobepeeledhas been transferred to the substrate for transfer at the same time as beingpeeled from the substrate . However, only the peeling of the layer to be peeled may be performed without using the substrate for transfer . Thereby, a functional film molded in a desired shape in advance, or a functional element containing a functional film and an electrode can be obtained. In addition, in the case where a material having cleavage characteristics is used as the separation layer, an external force may be applied to the
separation layer by applying physical stimulation (e.g., impact) to the side surface of the separation layer or the like.
The substrate (101, 201, 301) to be used in the above-mentioned first to third embodiments can be reused by removing the residual separation layer by cleansing, etching or the like after peeling the layer to be peeled. Therefore, a number of the substrates can be suppressed and the cost of manufacture can be reduced.
INDUSTRIAL APPLICABILITY
The present invention can be applied to memory elements, piezoelectric elements, pyroelectric elements, passive elements such as capacitors, optical elements, superconducting elements, photoelectric conversion elements , micromagneticelements andsemiconductorelements containing functional materials such as dielectric materials, piezoelectric materials , pyroelectric materials , magnetic material and semiconductor materials , and instruments to which those elements are applied.
Claims
1. A structure for functional film pattern formation comprising: a substrate (101, 201, 301) in which a predetermined pattern is formed; a separation layer (102 , 202 , 302) directly or indirectly provided on said substrate (101, 201, 301) ; and a layer to be peeled (103, 105, 106, 203, 303) provided on said separation layer (102, 202, 302) and containing a functional film (103, 105b, 106a, 203, 303) formed by using a functional material; wherein said layer to be peeled (103, 105, 106, 203,
303) is peeled from said substrate (101, 201, 301) or bonding strength between said layer to be peeled (103, 105, 106, 203,
303) and said substrate (101, 201, 301) becomes lower by one of heating said separation layer (102) , applying an electromagnetic wave toward said separation layer (202) , and applying an external force to said separation layer (302) . 2. A structure for functional film pattern formation according to claim 1, wherein said separation layer (102) contains an inorganicmaterial which is decomposed to generate a gas by being heated.
3. A structure for functional film pattern formation according to claim 1, wherein said separation layer (202) contains an inorganicmaterial which is decomposedto generate a gas by being applied with an electromagnetic wave.
4. A structure for functional film pattern formation according to claim 2 or 3 , wherein said separation layer (102 , 202) contains at least one of carbonate, sulfate and nitrate.
5. A structure for functional film pattern formation according to claim 4, wherein said separation layer (102,
202) contains at least one of magnesium carbonate (MgCO3) , calcium carbonate (CaCO3) , strontium carbonate (SrCO3) , barium carbonate (BaCO3) , lithium carbonate (LiCO3) , sodium carbonate (Na2CO3) , potassium carbonate (K2CO3) , magnesium sulfate (MgSO4) , calcium sulfate (CaSO4) , strontium sulfate (SrSO4) , barium sulfate (BaSO4) , iron sulfate (FeSO4) , cobalt sulfate (CoSO4) , nickel sulfate (NiSO4) , zinc sulfate (ZnSO4) , lead sulfate (PbSO4), bismuth sulfate (Bi (SO4) 3) , strontium nitrate (Sr (NO3) 2) and cesium nitrate (CsNO3). 6. A structure for functional film pattern formation according to claim 1, wherein said separation layer (102) contains an inorganic material which reacts with one of a component in an atmosphere and a component contained in an adjacent layer to generate a gas by being heated. 7. A structure for functional film pattern formation according to claim 1, wherein said separation layer (202) contains an inorganic material which reacts with one of a component in an atmosphere and a component contained in an adjacent layer to generate a gas by being applied with an electromagnetic wave.
8. A structure for functional film pattern formation according to claim 6 or 7 , wherein said Reparation layer (102 ,
202) contains at least one of metal nitride, metal carbide and metal sulfide.
9. A structure for functional film pattern formation according to any one of claims 2 to 8, further comprising: an electromagnetic wave absorbing layer (210) provided between said substrate (101, 201) and said separation layer (102, 202) and formed by using a material which absorbs an electromagnetic wave to generate heat.
10. A structure for functional film pattern formation according to claim 9, wherein said electromagnetic wave absorbing layer (210) contains one of carbon, ceramics and glass .
11. A structure for functional film pattern formation according to claim 1, wherein said separation layer (302) contains a material having cleavage characteristics .
12. A structure for functional film pattern formation according to claim 11, wherein said separation layer (302) contains boron nitride.
13. A structure for functional film pattern formation according to claim 11, wherein said separation layer (302) contains at least one of mica, graphite, and transition metal chalcogenide including molybdenum disulfide (MoS2) .
14. A structure for functional film pattern formation according to any one of claims 1 to 13 , wherein said substrate (101, 201, 301) contains one of a single crystal material, which includes one of an oxide single crystal material and
' a semiconductor single crystal material , a ceramics material
and a glass material .
15. A structure for functional film pattern formation according to any one of claims 2, 6 and 11-14, wherein said substrate (101, 201, 301) contains a metal material. 16. A structure for functional film pattern formation according to any one of claims 1 to 15 , wherein said functional film (103, 105b, 106a, 203, 303) contains at least one of a piezoelectric material, a pyroelectric material and a ferroelectric material . 17. A structure for functional film pattern formation according to any one of claims 1 to 15 , wherein said functional film (103, 105b, 106a, 203, 303) contains a superconducting material .
18. A structure for functional film pattern formation according to any one of claims 1 to 15 , wherein said functional film (103, 105b, 106a, 203, 303) contains amagneticmaterial .
19. A structure for functional film pattern formation according to any one of claims 1 to 15 , wherein said functional film (103, 105b, 106a, 203, 303) contains a semiconductor material.
20. A structure for functional film pattern formation according to any one of claims 1 to 19, wherein said layer to be peeled (105, 106) has a functional film (105b, 106a) and at least one electrode layer (105a, 106b) formed on at least one of an upper surface and a lower surface of the functional film (105b, 106a) . " 21. A method of manufacturing a functional film comprising
the steps of :
(a) preparing a substrate (101, 201, 301) in which a predetermined pattern is formed;
(b) forming a separation layer (102, 202, 302) directly or indirectly on said substrate (101, 201, 301);
(c) forming a layer to be peeled (103, 105, 106, 203, 303) containing a functional film (103, 105b, 106a, 203, 303) , which is formed by using a functional material, on said separation layer (102, 202, 302); and (d) peeling said layer to be peeled (103, 105, 106, 203, 303) from said substrate (101, 201, 301) or reducing bonding strength between said layer to be peeled (103, 105, 106, 203, 303) and said substrate (101, 201, 301) by one of heating said separation layer (102) , applying an electromagnetic wave toward said separation layer (202) , and applying an external force to said separation layer (302) .
22. A method of manufacturing a functional film according to claim 21, wherein said separation layer (102) contains an inorganic material which is decomposed to generate a gas by being heated.
23. A method of manufacturing a functional film according to claim 21, wherein said separation layer (202) contains an inorganic material which is decomposed to generate a gas by being applied with an electromagnetic wave. 24. A method of manufacturing a functional film according to claim 22 or 23, wherein said separation layer (102, 202) contains at least one of carbonate, sulfate and nitrate.
25. A method of manufacturing a functional film according to claim 24, wherein said separation layer (102, 202) contains at least one ofmagnesium carbonate (MgCO3) , calcium carbonate (CaCO3) , strontiumcarbonate (SrCO3) , bariumcarbonate (BaCO3) , lithium carbonate (LiCO3) , sodium carbonate (Na2CO3) , potassium carbonate (K2CO3) , magnesium sulfate (MgSO4) , calcium sulfate (CaSO4) , strontium sulfate (SrSO4) , barium sulfate (BaSO4) , iron sulfate (FeSO4) , cobalt sulfate (CoSO4) , nickel sulfate (NiSO4) , zinc sulfate (ZnSO4) , lead sulfate (PbSO4), bismuth sulfate (Bi(SO4J3), strontium nitrate
(Sr(NO3J2) and cesium nitrate (CsNO3) .
26. A method of manufacturing a functional film according to claim 21, wherein said separation layer (102) contains an inorganic material which reacts with one of a component in an atmosphere and a component contained in an adjacent layer to generate a gas by being heated.
27. A method of manufacturing a functional film according to claim 21, wherein said separation layer (202) contains an inorganic material which reacts with one of a component in an atmosphere and a component contained in an adjacent layer togenerateagasbybeingappliedwithanelectromagnetic wave.
28. A method of manufacturing a functional film according to claim 26 or 27, wherein said separation layer (102, 202) contains at least one of metal nitride, metal carbide and metal sulfide . '29. A method of manufacturing a functional film according
to any one of claims 22 to 28, further comprising, prior to step (b) , the step of: forming an electromagnetic wave absorbing layer (210) on said substrate (101 , 201) by using a material which absorbs an electromagnetic wave to generate heat.
30. A method of manufacturing a functional film according to claim29 , wherein saidelectromagneticwave absorbing layer (210) contains one of carbon, ceramics and glass.
31. A method of manufacturing a functional film according to claim 23 or 27, wherein step (d) includes applying an ultraviolet ray toward said separation layer (202) .
32. A method of manufacturing a functional film according to any one of claims 23 , 27 , 29 and 30 , wherein step (d) includes applying an infrared ray toward one of said separation layer (202) and said electromagnetic wave absorbing layer (210) .
33. A method of manufacturing a functional film according to any one of claims 23 , 27 , 29 and 30 , wherein step (d) includes applying amicrowave toward one of said separation layer (202) and said electromagnetic wave absorbing layer (210) . 34. A method of manufacturing a functional film according to claim 21, wherein said separation layer (302) contains a material having cleavage characteristics.
35. A method of manufacturing a functional film according to claim 34, wherein said separation layer (302) contains boron nitride.
36. A method of manufacturing a functional film according to claim 34, wherein said separation layer (302) contains
at least one of mica, graphite, and transition metal chalcogenide including molybdenum disulfide (MoS2) . 37. A method of manufacturing a functional film according to any one of claims 21 to 36, wherein said substrate (101, 201, 301) contains one of a single crystal material, which includes one of an oxide single crystal material and a semiconductor single crystal material, a ceramics material and a glass material .
38. A method of manufacturing a functional film according to any one of claims 22, 26 and 34-36, wherein said substrate
(101, 201, 301) contains a metal material.
39. A method of manufacturing a functional film according to any one of claims 21 to 38, wherein said functional film (103, 105b, 106a, 203, 303) contains at least one of a piezoelectric material , a pyroelectric material and a ferroelectric material .
40. A method of manufacturing a functional film according to any one of claims 21 to 38, wherein said functional film (103, 105b, 106a, 203, 303) contains a superconducting material.
41. A method of manufacturing a functional film according to any one of claims 21 to 38, wherein said functional film (103, 105b, 106a, 203, 303) contains a magnetic material.
42. A method of manufacturing a functional film according to any one of claims 21 to 38, wherein said functional film
(103, 105b, 106a, 203, 303) contains a semiconductormaterial. ' 43. A method of manufacturing a functional film according
to any one of claims 21 to 42 , wherein step (c) includes forming an electrode layer (105a) on said separation layer (102, 202, 302) , and forming the functional film (105b) on saidelectrode layer (105a) . 44. A method of manufacturing a functional film according to any one of claims 21 to 43 , wherein step (c) includes forming an electrode layer (106b) on the functional film (106a) formed directly or indirectly on said separation layer (102, 202, 302) . 45. A method of manufacturing a functional film according to any one of claims 21 to 44, further comprising, prior to step (d) , the step of:
(c1) providing a second substrate (104, 204, 304) on said layer to be peeled (103, 105, 106, 203, 303); wherein step (d) includes peeling said layer to be peeled (103, 105, 106, 203, 303) from said substrate (101, 201, 301) and transferring said layer to said second substrate (104, 204, 304) . 46. A method of manufacturing a functional film according to claim 45, wherein step (c1) includes fixing said second substrate (104, 204, 304) to said layer to be peeled (103, 105, 106, 203, 303) by using an adhesive agent.
Priority Applications (3)
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EP06747255A EP1889306B1 (en) | 2005-06-07 | 2006-06-05 | Structure for functional film pattern formation and method of manufacturing functional film |
DE602006020865T DE602006020865D1 (en) | 2005-06-07 | 2006-06-05 | STRUCTURE FOR FORMING A PATTERN FOR A FUNCTIONAL FILM AND METHOD FOR PRODUCING THE FUNCTIONAL FILM |
US11/885,279 US20080135162A1 (en) | 2005-06-07 | 2006-06-05 | Structure for Functional Film Pattern Formation and Method of Manufacturing Functional Film |
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EP (1) | EP1889306B1 (en) |
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EP2555269A1 (en) * | 2010-03-31 | 2013-02-06 | Panasonic Corporation | Method for manufacturing ferroelectric device |
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EP1889307B1 (en) * | 2005-06-07 | 2011-04-20 | FUJIFILM Corporation | Functional film containing structure and method of manufacturing functional film |
US20110109203A1 (en) * | 2009-11-06 | 2011-05-12 | The Trustees Of Princeton University | Flexible piezoelectric structures and method of making same |
WO2011127258A1 (en) * | 2010-04-07 | 2011-10-13 | Massachusetts Institute Of Technology | Fabrication of large-area hexagonal boron nitride thin films |
TWI644800B (en) * | 2018-01-15 | 2018-12-21 | 國立臺灣師範大學 | Biological sensing chip containing molybdenum disulfide and detection device using the biological sensing chip |
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US4886573A (en) * | 1986-08-27 | 1989-12-12 | Hitachi, Ltd. | Process for forming wiring on substrate |
US4988674A (en) * | 1989-02-09 | 1991-01-29 | Eastman Kodak Company | Electrically conductive articles and processes for their fabrication |
US6071795A (en) * | 1998-01-23 | 2000-06-06 | The Regents Of The University Of California | Separation of thin films from transparent substrates by selective optical processing |
JP2002134806A (en) * | 2000-10-19 | 2002-05-10 | Canon Inc | Piezoelectric film actuator, liquid injection head, and method of manufacturing the same |
US6589857B2 (en) * | 2001-03-23 | 2003-07-08 | Matsushita Electric Industrial Co., Ltd. | Manufacturing method of semiconductor film |
FR2830983B1 (en) * | 2001-10-11 | 2004-05-14 | Commissariat Energie Atomique | METHOD FOR MANUFACTURING THIN FILMS CONTAINING MICROCOMPONENTS |
CN1263173C (en) * | 2001-12-06 | 2006-07-05 | 松下电器产业株式会社 | Composite piezoelectric body and making method thereof |
DE102004058431B4 (en) * | 2003-12-05 | 2021-02-18 | Infineon Technologies Americas Corp. | III-nitride semiconductor device with trench structure |
US7943491B2 (en) * | 2004-06-04 | 2011-05-17 | The Board Of Trustees Of The University Of Illinois | Pattern transfer printing by kinetic control of adhesion to an elastomeric stamp |
JP4949668B2 (en) * | 2004-12-09 | 2012-06-13 | 富士フイルム株式会社 | Manufacturing method of ceramic film and structure including ceramic film |
EP1889307B1 (en) * | 2005-06-07 | 2011-04-20 | FUJIFILM Corporation | Functional film containing structure and method of manufacturing functional film |
DE602006021014D1 (en) * | 2005-06-07 | 2011-05-12 | Fujifilm Corp | STRUCTURE CONTAINING FUNCTIONAL FILM AND METHOD FOR PRODUCING A FUNCTIONAL FILM |
US20090053478A1 (en) * | 2005-06-07 | 2009-02-26 | Fujifilm Corporation | Functional film containing structure and method of manufacturing functional film |
US20060288928A1 (en) * | 2005-06-10 | 2006-12-28 | Chang-Beom Eom | Perovskite-based thin film structures on miscut semiconductor substrates |
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EP2555269A4 (en) * | 2010-03-31 | 2014-05-14 | Panasonic Corp | Method for manufacturing ferroelectric device |
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