NZ716340B2 - Circuits and substrates fabricated using a method of forming a conductive image on a non-conductive surface - Google Patents
Circuits and substrates fabricated using a method of forming a conductive image on a non-conductive surface Download PDFInfo
- Publication number
- NZ716340B2 NZ716340B2 NZ716340A NZ71634012A NZ716340B2 NZ 716340 B2 NZ716340 B2 NZ 716340B2 NZ 716340 A NZ716340 A NZ 716340A NZ 71634012 A NZ71634012 A NZ 71634012A NZ 716340 B2 NZ716340 B2 NZ 716340B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- metal coordination
- coordination complex
- metal
- magnetic field
- substrate
- Prior art date
Links
- 239000000758 substrate Substances 0.000 title claims abstract description 93
- 238000000034 method Methods 0.000 title claims abstract description 71
- 229910052751 metal Inorganic materials 0.000 claims abstract description 199
- 239000002184 metal Substances 0.000 claims abstract description 199
- 150000004696 coordination complex Chemical class 0.000 claims abstract description 114
- 230000005291 magnetic effect Effects 0.000 claims abstract description 53
- 238000000151 deposition Methods 0.000 claims abstract description 48
- 239000004020 conductor Substances 0.000 claims abstract description 18
- 238000001035 drying Methods 0.000 claims abstract description 18
- 230000005670 electromagnetic radiation Effects 0.000 claims abstract description 15
- 230000003213 activating effect Effects 0.000 claims abstract description 11
- 239000003446 ligand Substances 0.000 claims description 7
- 238000005530 etching Methods 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 239000000243 solution Substances 0.000 description 20
- 230000005855 radiation Effects 0.000 description 17
- 239000000463 material Substances 0.000 description 15
- 239000000126 substance Substances 0.000 description 14
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- 230000008569 process Effects 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 9
- 230000008021 deposition Effects 0.000 description 9
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 8
- 229920000106 Liquid crystal polymer Polymers 0.000 description 8
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 8
- 229910052802 copper Inorganic materials 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- 238000012545 processing Methods 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 239000004642 Polyimide Substances 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000003638 chemical reducing agent Substances 0.000 description 7
- 150000002500 ions Chemical class 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229920001721 polyimide Polymers 0.000 description 7
- 239000010408 film Substances 0.000 description 6
- 238000010329 laser etching Methods 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 235000012431 wafers Nutrition 0.000 description 6
- 230000004888 barrier function Effects 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000008367 deionised water Substances 0.000 description 5
- 229910021641 deionized water Inorganic materials 0.000 description 5
- 230000001590 oxidative effect Effects 0.000 description 5
- 238000001020 plasma etching Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 3
- 238000003486 chemical etching Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000008139 complexing agent Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- QLOKJRIVRGCVIM-UHFFFAOYSA-N 1-[(4-methylsulfanylphenyl)methyl]piperazine Chemical compound C1=CC(SC)=CC=C1CN1CCNCC1 QLOKJRIVRGCVIM-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- FRHBOQMZUOWXQL-UHFFFAOYSA-L ammonium ferric citrate Chemical compound [NH4+].[Fe+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O FRHBOQMZUOWXQL-UHFFFAOYSA-L 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 238000000407 epitaxy Methods 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 239000004313 iron ammonium citrate Substances 0.000 description 2
- 235000000011 iron ammonium citrate Nutrition 0.000 description 2
- 238000001459 lithography Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 2
- 230000005298 paramagnetic effect Effects 0.000 description 2
- 238000000059 patterning Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- 229910001961 silver nitrate Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- VEHXKUNAGOJDJB-UHFFFAOYSA-N (4-formyl-2-methoxyphenyl) 4-methoxybenzoate Chemical compound C1=CC(OC)=CC=C1C(=O)OC1=CC=C(C=O)C=C1OC VEHXKUNAGOJDJB-UHFFFAOYSA-N 0.000 description 1
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- ZEYKLMDPUOVUCR-UHFFFAOYSA-N 2-chloro-5-(trifluoromethyl)benzenesulfonyl chloride Chemical compound FC(F)(F)C1=CC=C(Cl)C(S(Cl)(=O)=O)=C1 ZEYKLMDPUOVUCR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- QZPSXPBJTPJTSZ-UHFFFAOYSA-N aqua regia Chemical compound Cl.O[N+]([O-])=O QZPSXPBJTPJTSZ-UHFFFAOYSA-N 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000012993 chemical processing Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- OJKANDGLELGDHV-UHFFFAOYSA-N disilver;dioxido(dioxo)chromium Chemical compound [Ag+].[Ag+].[O-][Cr]([O-])(=O)=O OJKANDGLELGDHV-UHFFFAOYSA-N 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000007772 electroless plating Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000005251 gamma ray Effects 0.000 description 1
- 230000003116 impacting effect Effects 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 229910001172 neodymium magnet Inorganic materials 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012811 non-conductive material Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- CIBMHJPPKCXONB-UHFFFAOYSA-N propane-2,2-diol Chemical compound CC(C)(O)O CIBMHJPPKCXONB-UHFFFAOYSA-N 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000005368 silicate glass Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- -1 that is Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000012876 topography Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/1601—Process or apparatus
- C23C18/1633—Process of electroless plating
- C23C18/1655—Process features
- C23C18/1664—Process features with additional means during the plating process
- C23C18/1673—Magnetic field
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/18—Pretreatment of the material to be coated
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/18—Pretreatment of the material to be coated
- C23C18/20—Pretreatment of the material to be coated of organic surfaces, e.g. resins
- C23C18/22—Roughening, e.g. by etching
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/288—Deposition of conductive or insulating materials for electrodes conducting electric current from a liquid, e.g. electrolytic deposition
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76801—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
- H01L21/76802—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing by forming openings in dielectrics
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76877—Filling of holes, grooves or trenches, e.g. vias, with conductive material
- H01L21/76879—Filling of holes, grooves or trenches, e.g. vias, with conductive material by selective deposition of conductive material in the vias, e.g. selective C.V.D. on semiconductor material, plating
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00
- H05K2203/10—Using electric, magnetic and electromagnetic fields; Using laser light
- H05K2203/104—Using magnetic force, e.g. to align particles or for a temporary connection during processing
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00
- H05K2203/11—Treatments characterised by their effect, e.g. heating, cooling, roughening
- H05K2203/1157—Using means for chemical reduction
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/10—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern
- H05K3/105—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern by conversion of non-conductive material on or in the support into conductive material, e.g. by using an energy beam
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/10—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern
- H05K3/18—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material
- H05K3/181—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material by electroless plating
- H05K3/182—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material by electroless plating characterised by the patterning method
- H05K3/185—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material by electroless plating characterised by the patterning method by making a catalytic pattern by photo-imaging
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/38—Improvement of the adhesion between the insulating substrate and the metal
- H05K3/381—Improvement of the adhesion between the insulating substrate and the metal by special treatment of the substrate
Abstract
Disclosed is a substrate fabricated using a method comprising the steps of: (a) activating at least a portion of a non-conductive substrate surface (10); (b) depositing a metal coordination complex (15) on a part of the activated portion of the surface (10); (c) subjecting the metal coordination complex (15) that is located on the part of the activated portion of the surface (10) to a magnetic field (25) to align molecules of the metal coordination complex (15) with the magnetic field (25) and thereby more deeply injecting the metal coordination complex (15) into the nonconductive substrate (10) than would occur in the step of depositing the metal coordination complex (15); (d) exposing the metal coordination complex (15) to electromagnetic radiation; (e) reducing the metal coordination complex (15) to elemental metal; (f) removing unreduced metal coordination complex (15) from the surface; (g) drying the surface; and (h)depositing a conductive material onto the surface. plex (15) that is located on the part of the activated portion of the surface (10) to a magnetic field (25) to align molecules of the metal coordination complex (15) with the magnetic field (25) and thereby more deeply injecting the metal coordination complex (15) into the nonconductive substrate (10) than would occur in the step of depositing the metal coordination complex (15); (d) exposing the metal coordination complex (15) to electromagnetic radiation; (e) reducing the metal coordination complex (15) to elemental metal; (f) removing unreduced metal coordination complex (15) from the surface; (g) drying the surface; and (h)depositing a conductive material onto the surface.
Description
CIRCUITS AND SUBSTRATES FABRICATED USING A METHOD OF
FORMING A CONDUCTIVE IMAGE ON A NON-CONDUCTIVE SURFACE
William Wismann
CROSS NCE TO RELATED APPLICATIONS
This ation is related to and claims the benefit of (1) U.S.
Provisional Patent Application No. 61/525,662, filed in the name of William
Wismann on August 19, 2011, (2) U.S. Provisional Patent Application No.
61/568,736, filed in the name of William Wismann on December 9, 2011, and
(3) is a continuation of U.S. Patent Application No. ,797, filed in the name
of William Wismann on February 23, 2012, all of which are hereby incorporated
herein by reference in their entirety.
[001a] The t ation has been d out of New Zealand
patent application 622408 (NZ 622408). In the description in this present
specification reference may be made to subject matter which is not within the
scope of the appended claims but relates to subject matter claimed in
NZ 622408. That subject matter should be readily fiable by a person
skilled in the art and may assist in putting into practice the invention as defined
in the presently appended claims.
FIELD
This invention relates to the field of electronic device
manufacture.
BACKGROUND
Conductive images on non-conductive or dielectric surfaces are
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ubiquitous in today’s technology-driven world. Perhaps the most widely known
example of such are the ated circuits found in virtually all electronic
devices. Integrated circuits result from a sequence of photographic and
chemical processing steps by which the circuits are gradually created on a
dielectric substrate such as a silicon wafer.
A typical wafer is made out of extremely pure silicon that is grown
into mono-crystalline cylindrical ingots, called boules, that are up to 300 mm in
diameter. The boules are then sliced into wafers about 0.75 mm thick and
polished to obtain a very smooth flat surface.
The formation of a circuit on a wafer requires numerous steps
that can be categorized into two major parts: end-of-line (FEOL)
processing and back- end-of-line (BEOL) processing.
FEOL processing refers to the formation of circuits directly in the
silicon. The raw wafer is first subjected to epitaxy, the growth of crystals of
ultrapure silicon on the wafer wherein the crystals mimic the orientation of the
substrate.
After epitaxy, front-end surface engineering generally consists of
the steps of growth of the gate tric, traditionally silicon dioxide (SiO2),
patterning of the gate, patterning of the source and drain s, and
uent implantation or ion of dopants to obtain the desired
mentary electrical properties. In dynamic random access memory
(DRAM) s, storage capacitors are also fabricated at this time, typically
stacked above the access stor.
Once the various semiconductor devices have been created, they
must be interconnected to form the desired electrical circuits, which comprise
the BEOL portion of the process. BEOL involves creating metal interconnecting
wires that are ed by dielectric layers. The insulating material was
traditionally a form of silicate glass, SiO2, but other low dielectric constant
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materials can be used.
The metal interconnecting wires often comprise um. In an
approach to wiring called subtractive aluminum, blanket films of aluminum are
deposited, patterned and etched to form the wires. A dielectric material is then
deposited over the exposed wires. The various metal layers are interconnected
by etching holes, called vias, in the ting material and depositing tungsten
in the holes. This approach is still used in the ation of memory chips such
as DRAMs as the number of interconnect levels is small.
More ly, as the number of interconnect levels has
increased due to the large number of transistors that now need to be
interconnected in a modern microprocessor, the timing delay in the wiring has
become significant, prompting a change in wiring al from aluminum to
copper and from the silicon dioxides to newer low-K material. The result is not
only enhanced performance but reduced cost as well in that damascene
processing is substituted for subtractive aluminum technology, thereby
elimination several steps. In damascene processing, the tric al is
deposited as a blanket film, which is then patterned and etched leaving holes or
trenches. In single damascene processing, copper is then deposited in the
holes or trenches surrounded by a thin barrier film resulting in filled vias or wire
lines. In dual damascene technology, both the trench and via are fabricated
before the deposition of copper resulting in formation of both vias and wire lines
simultaneously, further reducing the number of processing steps. The thin
barrier film, called copper barrier seed (CBS), is necessary to prevent copper
diffusion into the dielectric. The ideal barrier film is as thin as possible. As the
presence of excessive r film competes with the available copper wire
cross section, formation of the thinnest uous barrier represents one of the
greatest g challenges in copper processing today.
As the number of interconnect levels increases, planarization of
the previous layers is required to ensure a flat surface prior to subsequent
lithography. Without it, the levels would become increasingly crooked and
extend outside the depth of focus of available lithography, interfering with the
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ability to pattern. CMP (chemical mechanical planarization) is a processing
method to achieve such planarization gh dry etch back is still mes
employed if the number of interconnect levels is low.
The above process, although described ically with regard to
n chip manufacture, is fairly generic for most types of printed circuits,
printed circuit boards, antennas, solar cells, solar thin films, nductors and
the like. As can be seen, the process is subtractive; that is a metal, usually
copper, is deposited uniformly over a substrate surface and then unwanted
metal, that is, metal that does not comprise some part of the final circuit, is
removed. A number of additive processes are known, which resolve some of
the problems associated with the ctive process but which engender
problems of their own, a significant one of which involves adherence of a builtup
conducting layer to the substrate.
What is needed is an additive process for integrated circuit
fabrication that has all of the advantages of other additive processes but which
exhibits improved adhesion properties to substrates. The current invention
provides such an additive process.
[013a] Alternatively or additionally, what is needed is at least a useful
choice for the public.
SUMMARY
In one aspect the invention comprises an analog circuit
fabricated using a method comprising the steps of:
activating at least a portion of a non-conductive substrate
surface;
depositing a metal coordination complex on a part of the
activated n of the surface;
subjecting the metal coordination complex that is located on the
part of the activated portion of the e to a magnetic field to align
molecules of the metal coordination x with the magnetic field and
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thereby more deeply injecting the metal coordination complex into the
nonconductive substrate than would occur in the step of depositing the metal
coordination x;
exposing the metal coordination complex to electromagnetic
radiation;
reducing the metal coordination x to elemental metal;
ng unreduced metal nation complex from the
surface;
drying the surface; and
depositing a conductive material onto the surface.
[014a] In another aspect the invention comprises a digital t
fabricated using a method comprising the steps of:
activating at least a portion of a non-conductive substrate surface;
ting a metal coordination complex on a part of the activated
portion of the surface;
subjecting the metal coordination complex that is located on the part of
the activated portion of the surface to a magnetic field to align molecules of
the metal coordination x with the magnetic field and thereby more
deeply injecting the metal coordination complex into the nonconductive
substrate than would occur in the step of depositing the metal coordination
exposing the metal coordination complex to electromagnetic radiation;
reducing the metal coordination complex to elemental metal;
removing unreduced metal nation complex from the surface;
drying the surface; and
depositing a conductive material onto the surface.
[014b] In another aspect the invention comprises a mixed-signal circuit
fabricated using a method comprising the steps of:
activating at least a portion of a non-conductive substrate surface;
depositing a metal nation complex on a part of the activated
portion of the surface;
subjecting the metal coordination complex that is located on the part of
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the activated portion of the surface to a magnetic field to align les of
the metal nation complex with the magnetic field and thereby more
deeply injecting the metal coordination complex into the nonconductive
substrate than would occur in the step of depositing the metal coordination
complex;
exposing the metal coordination complex to electromagnetic ion;
reducing the metal coordination complex to elemental metal;
removing unreduced metal coordination complex from the surface;
drying the surface; and
depositing a tive material onto the surface.
[014c] In another aspect the invention comprises an RF circuit
fabricated using a method comprising the steps of:
activating at least a portion of a non-conductive substrate surface;
depositing a metal coordination complex on a part of the ted
portion of the surface;
subjecting the metal coordination x that is located on the part of
the activated portion of the surface to a magnetic field to align molecules of
the metal coordination complex with the magnetic field and thereby more
deeply injecting the metal nation complex into the nonconductive
substrate than would occur in the step of depositing the metal coordination
complex;
exposing the metal coordination complex to electromagnetic radiation;
reducing the metal coordination x to elemental metal;
removing unreduced metal coordination complex from the surface;
drying the surface; and
depositing a conductive material onto the e.
[014d] In another aspect the ion comprises a substrate fabricated
using a method comprising the steps of:
activating at least a portion of a non-conductive substrate surface;
depositing a metal coordination complex on a part of the activated
portion of the surface;
subjecting the metal coordination complex that is located on the part of
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the activated portion of the surface to a ic field to align molecules of
the metal coordination complex with the magnetic field and thereby more
deeply injecting the metal coordination complex into the nonconductive
substrate than would occur in the step of depositing the metal coordination
complex;
exposing the metal nation complex to electromagnetic radiation;
reducing the metal coordination complex to elemental metal;
removing unreduced metal coordination complex from the surface;
drying the surface; and
depositing a conductive material onto the surface.
[014e] Further aspects are described and d in NZ .
[014f] Described herein is a method of forming a conductive layer on a
surface, comprising:
activating at least a portion of a non-conductive substrate surface;
applying a magnetic field to the surface;
depositing a metal coordination complex on at least a part of the
activated portion of the surface;
removing the magnetic field;
exposing the metal coordination complex to electromagnetic radiation;
reducing the metal coordination complex to elemental metal; removing
unreduced metal nation complex from the surface; drying the surface; and
depositing a conductive material onto the surface.
In an aspect, activating the substrate surface comprises etching
the surface.
In an , g the surface comprises chemical etching.
In an aspect, chemical etching comprises acid g, base
etching or oxidative etching.
In an aspect, etching the e comprises mechanical etching.
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In an aspect, etching the surface comprises plasma etching.
In an aspect, etching the surface comprises laser- etching.
In an aspect, plasma or laser etching comprises etching in a predetermined
pattern.
In an aspect, the ic field has a magnetic flux density of at
least 1000 gauss.
In an aspect, the magnetic field is orthogonal to the surface.
In an aspect, depositing a metal coordination complex on at least
a portion of the surface comprises using a mask.
In an aspect, the mask ses an electronic circuit.
In an , the electronic circuit is selected from the group
consisting of an analog circuit, a digital circuit, a mixed-signal circuit and an RF
circuit.
Described herein is an analog circuit fabricated using the method
described herein.
Described herein is a digital circuit fabricated using the method
described herein.
Described herein is a mixed-signal t ated using the
method described herein.
bed herein is an RF circuit fabricated using the method
described herein.
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In an aspect, exposing the metal coordination complex to
electromagnetic radiation ses microwave radiation, infrared radiation,
visible light radiation, ultraviolet radiation, X-ray radiation or gamma radiation.
In an aspect, reducing the metal coordination complex to a zero
oxidation state metal comprises using a combination of metals and/or catalysts.
In an aspect, removing ced metal coordination complex
from the surface comprises washing the surface with a solvent.
In an aspect, drying the surface comprises drying at ambient
temperature or drying at elevated temperature.
In an aspect, drying the surface at ambient or elevated
temperature comprises using a vacuum chamber.
In an aspect, depositing a conductive material onto the surface
ses electrolytic deposition of a metal onto the portion of the surface
comprising the reduced metal coordination x.
In an aspect, electrolytic deposition of a metal onto the portion of
the surface comprising the reduced metal coordination complex comprises:
contacting a ve terminal of a direct t power supply with at
least the portion of the surface comprising the reduced metal coordination
complex;
ing an aqueous solution comprising a salt of the metal to be
deposited, an electrode made of the metal immersed in the aqueous solution or
a ation thereof;
contacting a positive terminal of the direct current power supply with the
aqueous solution;
ting at least the portion of the surface sing the reduced
metal coordination complex with the aqueous solution; and
turning on the power supply.
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In an aspect, ting a conductive material onto the surface
comprises electroless deposition of a metal onto the portion of the surface
sing the d metal nation complex.
In an aspect, electrolessly depositing a metal onto the portion of
the surface comprising the reduced metal coordination x comprises
contacting at least the portion of the surface comprising the metal coordination
complex with a on comprising a salt of the metal, a complexing agent and
a reducing agent.
In an aspect, depositing a conductive material onto the surface
ses deposition of a non-metallic conductive substance onto the portion of
the surface sing the reduced metal coordination complex.
In an aspect, the non-metallic conductive material is deposited
onto the portion of the surface comprising the reduced metal coordination
complex by electrostatic dispersion.
In an aspect, the entire non-conductive substrate surface is
activated and the metal coordination complex is deposited onto the entire
surface.
In an aspect, the entire non-conductive substrate surface is
activated and the metal coordination complex is deposited on a part of the
activated surface.
DETAILED DESCRIPTION
Brief description of the figures
The figure herein is provided solely to assist in the understanding
of the present invention and is not intended nor is it to be construed as limiting
the scope of this invention in any manner whatsoever.
Figure 1 shows a ate to be processed using the method of
this invention where the substrate is situated in an magnetic field such that the
field is orthogonal to the plane of the surface of the substrate.
8190808_2.docx
Discussion
It is understood that, with regard to this description and the
appended claims, reference to any aspect of this invention made in the singular
includes the plural and vice versa unless it is expressly stated or unambiguously
clear from the context that such is not ed.
As used herein, any term of approximation such as, without
limitation, near, about, approximately, substantially, essentially and the like,
mean that the word or phrase modified by the term of imation need not
be exactly that which is written but may vary from that written description to
some extent. The extent to which the description may vary will depend on how
great a change can be instituted and have one of ordinary skill in the art
recognize the ed version as still having the properties, characteristics and
capabilities of the word or phrase unmodified by the term of approximation. In
general, but with the preceding discussion in mind, a numerical value herein
that is modified by a word of approximation may vary from the stated value by
±10%, unless expressly stated ise.
As used herein, the use of “preferred,” “preferably,” or “more
preferred,” and the like refers to preferences as they d at the time of filing
of this patent application.
As used herein, a “conductive layer” refers to an electrically
conductive surface, for example, t limitation, a printed circuit.
As used herein, a onductive substrate” refers to a substrate
made of an electrically non-conductive material, sometimes referred to as an
insulator or a dielectric. Such materials include, without limitation, minerals
such as , alumina, magnesia, zirconia and the like, glass and most plastics.
Specific non-limiting examples include FR4, which is the general grade
designation for fiberglass reinforced epoxy resin such as, without limitation,
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DuPont Kapton® PV9103 polyimide and ULTRALAM® liquid crystal polymer
(Rogers Corporation, Chandler AZ).
As used herein, to “activate a non-conductive substrate surface,”
or a portion thereof of, refers to rendering the surface more amenable to
interaction with and subsequent physical or chemical g to another
material that is disposed onto the surface of the substrate. In an embodiment of
this invention, the other al can comprise a metal coordination complex. In
addition, altering the surface properties also refers to rendering the surface
more diffusive toward incident electromagnetic radiation. Altering the surface
properties can be accomplished by altering the aphy or the permeability
of the surface or a combination of the two. The topography of the surface can
be altered by mechanical or al means or a combination of the two.
Mechanical means of ng the surface properties of the
substrate include, t limitation, simple abrasion of the surface such as with
sandpaper or another abrasive al, rasping the surface with a file, g
the surface with a sharp object such as, t limitation, a tool bit, and laser
etching. ations of these and any other methods that result in an
abraded surface are within the scope of this invention.
In some embodiments, the surface may be prepared ab initio
using a mold that includes an abraded surface contour and forming the
substrate with altered surface properties by disposing a molten polymer into the
mold. When removed, the molded object will have an altered surface as
compared to an object molded using a smooth-surfaced mold. These methods
of altering a surface property are well-known to those skilled in the art and
require no further description,
Chemical means of altering the surface properties of a substrate
include, without limitation, acid etching, base etching, oxidative etching and
plasma g.
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Acid etching, as the name implies, refers to the use of a strong
acid such as sulfuric acid, hydrochloric acid and nitric acid. A e of
hydrochloric acid with nitric acid produces aqua regia, an ely strong acid
which can be used to alter the surface properties of a substrate. Most
commonly, however, the surface to be acid etched is a glass and the acid use to
etch the glass is hydrofluoric acid. This, and other acid etching technologies are
well-known in the art and likewise require no detailed explanation.
Base etching is the converse of acid g and involves the use
of a basic nce to alter the topology of the surface of a substrate. Many
organic polymers are susceptible to chemical ution with basic substances.
For instance, without limitation, potassium hydroxide will react with ters,
polyimides and oxides to alter their e properties. Other materials
tible to base etching will be known those skilled in the art. All such
materials are within the scope of this invention.
Oxidative etching refers to the alteration of the surface properties
of a substrate by contacting the surface with a strong oxidant which as, without
limitation, potassium permanganate.
Plasma g refers to the process of impacting the surface of a
substrate with a high-speed stream of a glow discharge of an appropriate gas.
The etching species may comprise charged ions or neutral atoms and radicals.
During the etch process, elements of the material being etched can chemically
react with the reactive species generated by the plasma. In addition, atoms of
the plasma- generating substance may imbed themselves at or just below the
surface of the substrate, further altering the properties of the surface. As with
the other methods of altering the properties of a surface, plasma etching is wellknown
in the art and needs no further description for the purposes of this
invention.
Laser etching is well-known in the art. Briefly, a laser beam is
ed at a surface that is within the laser's focal plane. The laser's movement
is controlled by a computer. As the laser focal point is moved across the
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surface, the material of the surface is, generally, vaporized thus g the
image being traced by the laser on the surface. With regard to this invention,
the laser may be used to impart an overall pattern on the surface of a substrate
or it may be used to trace the actual image to eventually be rendered
conductive onto the substrate.
Another means of altering the surface properties of a substrate
involves exposing the surface of the substrate to a fluid that is know of found to
soften the e, often with concomitant swelling of the surface. When a
coating material is applied to the swollen surface, the material can physically
ct at the boundary between it and the swollen surface, which can result
the material being more tightly bound to the surface, in particular when the
coated substrate is dried.
As used herein, "applying an magnetic field" to a substrate
surface involves placing a surface of the substrate on or near a source of a
magnetic field. The magnetic field may be ted by either a permanent
magnet, an electromagnet or a combination thereof. A single magnet or
plurality of magnets may be used. The e of the ate that is in contact
with or near the magnet may be the surface opposite to that surface onto which
a metal coordination complex is to be deposited or it may be the surface onto
which a metal coordination complex is to be deposited. That is, the source of
the magnetic field may be above or below the substrate wherein " refers
to the ted surface of the substrate and "below" refers to the surface
opposite the ted surface. If the magnetic field is generated using a
permanent , any type of magnet may be used so long as the field
strength is at least 1000 gauss, more preferably at least 2000 gauss. A
presently preferred permanent magnet is a neodymium magnet. It is also
preferred that a permanent magnet have dimensions such that close to or all of
the activated surface of the substrate is contained within the dimensions of the
magnet. Such an arrangement is shown in Fig. 1. In Fig. 1, substrate 10 has
an ted surface 15. Permanent magnet 20 is ed below substrate 10
and positioned such that the magnetic field generated by the magnet is
orthogonal to activated surface 15, which is a presently preferred configuration.
8190808_2.docx
As used herein, a "paramagnetic or ferromagnetic metal
coordination complex" is understood to have the meaning that would be
ascribed to these classes of metal complexes by those skilled in the art. The
metal coordination complex must be ferro- or para- magnetic so that, when
disposed on the surface of the substrate, it is affected by the orthogonal
magnetic field. Without being held to any particular theory, it is ed that the
complex, under the influence of the magnetic field, will either be drawn in toto
toward the source of the magnetic field and thereby be more deeply injected
into the e of the substrate or the field may cause the ligands of the
complex to align with the magnetic field thereby drawing the ligands further into
the substrate. A combination of the two processes may also occur. The result
in any case would be more tightly bound complex than that which would be
obtained without the influence of the magnetic field.
After the metal coordination complex is applied to the surface of
the substrate under the influence of the d magnetic field, the source of the
magnetic field is removed.
The metal coordination complex coated substrate is then d
to electromagnetic radiation to activate the metal coordination x toward a
reducing agent. As used herein, electromagnetic radiation includes virtually the
entire spectrum of such, i.e., microwave, infrared, e, iolet, X-ray and
gamma ray radiation. The composition of the metal coordination complex can
be manipulated to render it sensitive to a particular range with the
electromagnetic spectrum or, if desired, sensitizer(s) may be added to the
complex when it is disposed on the substrate to render the complex
ensitive or, if the complex is inherently photosensitive, to render it even
more so. As used here, "photosensitive" has its dictionary definition: ive
or responsive to light or other radiant energy, which would include each of the
types of radiation mentioned above.
Exposure to ion renders a portion of the metal coordination
complex susceptible to reduction. The reducing agent will reduce the metal
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coordination complex to elemental metal. The reducing agent can be any
metal- inclusive salt wherein the metal has a reduction ial that is greater,
i.e., conventionally has a more negative reduction potential than the metal of the
coordination complex. The following chart shows the reduction ial of a
number of common substances. Substances higher on the list are capable of
reduction of those beneath it.
8190808_2.docx
Reducing agent Reduction potential (V)
Li −3.04
Na −2.71
Mg −2.38
Al −1.66
H2(g) + 2OH − −0.83
Cr −0.74
Fe −0.44
H2 0.00
Sn2+ +0.15
Cu+ +0.16
Ag +0.80
2Br− +1.07
2Cl− +1.36
Mn2+ + 4H2O +1.49
The elemental metal resulting from the ion step is, of
course, insoluble in most ts. Thus, g the surface of the substrate
with an appropriate t, which is determined by the composition of the initial
metal coordination complex, will remove unexposed complex leaving the metal.
The metal may be evenly dispersed over the surface of the substrate if the
surface of the substrate was generally exposed or the metal may form a
te pattern if the substrate surface was d through a mask. A mask
is simply a material that is placed between the source of the electromagnetic
radiation and the surface of the substrate and which includes an image is to be
transferred to the surface of the substrate. The image may be a negative image
in which case the portions of the substrate surface that receive radiation
corresponds to those portions of the mask that are transparent to the particular
radiation or the image may be a positive image in which case the portions of the
substrate surface that receive radiation correspond to those portions outside the
8190808_2.docx
image areas of the mask.
Once the unexposed metal coordination complex is removed, the
substrate with is dried to complete formation of the metal image.
The metal image can be used as is, plated with another metal or
coated with a non-metallic conductive material.
If the metal image is to be plated with another metal, such can be
accomplished electrolytically or electrolessly. In this manner a conductive metal
layer is formed only on the regions of the image comprising the metal image,
the result being a raised conductive surface.
Electroless plating of the metal image portions of the surface of
the ate can be accomplished, without tion, by ting the surface
with a solution of a salt of a metal to be deposited in the presence of a
complexing agent to keep the metal ions in solution and to stabilize the solution
generally. The e with the complexed metal salt in contact with it or at
least near the surface is simultaneously or consecutively contacted with an
s solution of a reducing agent. The metal complex is reduced to afford
elemental metal which adheres to the metal image already on the surface of the
substrate; i.e., an electrolessly deposited layer of metal on metal results.
The metal complex solution and the reducing solution can be
concurrently sprayed onto the patterned substrate either from te spray
units, the spray streams being directed so as to intersect at or near the
substrate surface, or from a single spray unit having separate reservoirs and
spray tip orifices, the two streams being mixed as they emerge from the spray
tip and impinge on the substrate surface.
The electrodeposition s contemplated herein is well-known
in the art and need not be extensively described. In brief, the tal metal
image is connected to the negative terminal (cathode) of a direct current power
source, which may simply be a y but, more commonly, is a rectifier. The
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anode, which constitutes the second metal to be deposited onto the first metal
image, is connected to the positive terminal (anode) of the power source. The
anode and cathode are electrically connected by means of an electrolyte
on in which the imaged metal surface is submersed or bathed as by
contact with a spray of the solution.
The electrolyte on contains dissolved metal salts of the
metal to be plated as well as other ions that render the olyte conductive.
When power is applied to the system, the metallic anode is
oxidized to produce cations of the metal to be deposited and the positively
charged cations migrate to the e, i.e., the metal image on the substrate
surface, where they are reduced to the zero valence state metal and are
deposited on the surface.
In an embodiment of this invention, a solution of cations of the
metal to be deposited can be prepared and the solution can be sprayed onto
the metalized uct.
The conductive material to be coated on the elemental metal
image may also comprise a non-metallic conductive substance such as, without
limitation, carbon or a tive polymer. Such materials may be deposited on
the metal image by techniques such as, without limitation, electrostatic powder
g and electrostatic dispersion coating, which may be conducted as a wet
(from solvent) or dry s. The process may be carried out by
electrostatically charging the metal image and then contacting the image with
nano- or micro- sized particles that have been electrostatically charged with the
opposite charge to that applied to the metal image. In addition, to further
ensure that only the metal image is coated, the non- conductive substrate may
be grounded to eliminate any possibility of an tive charge developing on
the substrate or the substrate may be charged with the same polarity charge as
the substance to be ted such that the substance is repelled by the
substrate.
8190808_2.docx
EXAMPLES
Example 1
1. DuPont Kapton PV9103 ide, in small sheets is chemically etched
using a mixture of 0.1 N KOH (5.6 grams potassium hydroxide per 1 liter of
deionized water (DI)) with a 60% by weight solution of isopropanol alcohol, for 2
to 4 minutes
2. The etched polyimide sheet is rinsed with DI water and dried for 30
minutes in an oven at 100 ºC.
3. 10 grams of ferric um oxalate are suspended in 25ml of DI water
(in the darkroom) (Solution 1).
4. 10 grams of ferric ammonium oxalate are mixed with 1.0 gram of
potassium chlorate and 25 ml of DI water (also in the darkroom) (Solution 2).
. 2.3 grams of ammonium tetrachloroplatinate(II) are mixes with 1.7
grams of m chloride and 2ml of DI water (Solution 3).
6. ons 1, 2, and 3 are mixed together in equal amounts.
7. The etched polyimide sheet is placed on a 2000 gauss magnet that has
dimensions larger than those of the polyimide sheet and the mixture of Step 6 is
applied thinly over the surface of the sheet (in the darkroom) with a sponge
brush.
8. The coated polyimide sheet was air dried for 30 minutes (alternatively
the coated sheet may be placed an oven at 40 ºC for about 5 minutes or until
dry).
9. A mask comprising the desired pull tab image was placed on top of the
coating
8190808_2.docx
. The masked surface of the polyimide sheet was exposed to an ASC365
iolet light source at full strength for no less than 3 minutes
11. The light source was removed, the mask was separated from the
substrate surface and the surface was rinsed for 5 minutes with DI water and
then placed in a ethylenediamine tetraacetic acid (EDTA) bath comprising 15
grams of EDTA per 1000ml of DI water 10 minutes.
12. The rinsed substrate was placed in an oven at 40 ºC for 5 minutes or
until dry.
13. The substrate was placed in a bath comprising Shipley Electroless
Cuposit 328 with 27.5% 328 (A-12.5%, L-12.5%, C-2.5%) and 72.5% DI 25 ºC
for 5 minute intervals to record plating.
14. The resulting copper-plated polymide was rinsed with DI water for 10
minutes and air dried for 30 minutes (or can be placed in an oven at 40 ºC for 5
minutes or until dry).
Example 2
1. A Rogers ULTRALAM 3000 liquid crystal polymer (LCP) sheet was
ally etched with Electro-Brits E-prep 102, approximately 5% by volume
(40 grams per liter of sodium ide)
2. The sheet was static rinsed followed by a double cascade rinse.
3. The rinsed etched sheet was then processed with E-Neutralizer and
then rinsed again.
4. The sheet was then dipped in a 10% on of ic acid for 10
seconds and rinsed.
8190808_2.docx
. 10 grams of silver nitrate were dissolved in 25 ml of DI water (in the
darkroom).
6. 5 grams of potassium chromate were mixed with 5 ml of DI water (in the
darkroom)
7. Drops of silver nitrate were added to the potassium chromate solution
until a red precipitate formed. The mixture was allowed to stand for 24 hours
and then was filtered and diluted to 100 ml with DI water (in the darkroom)
8. The sheet was then placed on a 2000 gauss magnet and the silver
chromate mixture was thinly applied to it (in the darkroom) with a sponge brush.
9. The coated sheet was placed in an oven at 40 ºC for 10 s or until
dry.
. A pull test designed mask was placed on the coated surface of the LCP
sheet.
11. The masked LPC sheet was then d to ultraviolet light from an
ASC365 ultraviolet light source for 5 minutes.
12. The UV light source was removed, the LCP sheet was separated from
the mask and rinsed for 5 minutes with DI water and then placed in an EDTA
bath (15 grams of EDTA, per 1000ml of DI water) for 10 minutes.
13. The LCP sheet was then rinsed with DI for 10 minutes and put it into an
oven at 40 ºC for 5 s or until dry.
14. The LCP sheet was then placed in a bath comprising Shipley Electroless
t 328 with 27.5% 328 (1-12.5%, L-12.5%, C-2.5%) and 72.5% deionized
water at 25 ºC for 5 minute intervals to record plating.
. The copper-plated LCP sheet was removed from the bath, rinsed for 10
8190808_2.docx
s and then placed in an oven at 40 ºC for 5 minutes until dry.
Example 3
1. A thin sheet (0.15" thickness) of FR4 was chemically etched with a 10%
solution of sulfuric acid for 3 minutes and then with a 6% solution of potassium
hydroxide.
2. The sheet was then rinsed with DI water.
3. 30 grams of ammonium ferric citrate (the green form, 7.5% ammonia,
% iron and 77.5% hydrated citric acid) was mixed with 35 ml of warm (50 ºC)
DI water (in the darkroom) and then made up to a final volume of 50 ml with DI
water in an amber bottle (in the darkroom).
4. 1.8 grams of ammonium chloride in 20 ml of hot (70-80 ºC) DI water was
mixed with stirring with 3 grams of palladium(II) chloride until dissolved, and
then made up to 25 ml by addition of DI water.
. The mixture was filtered and bottled when cool.
6. 6 drops of the ammonium ferric citrate was added to 1 drop of palladium
chloride solution in a beaker until 20 ml of solution is obtained (in the darkroom).
7. The FR4 sheet was placed on a 2000 gauss magnet with dimensions
larger than those of the FR4 sheet and the nated complex solution was
sponge brushed thinly on the surface of the sheet (in the darkroom).
8. The FR4 sheet was then place in an oven at 40 ºC for 10 s or
until dry.
9. A pull test ed mask was then placed on the treated surface of the
FR4 sheet.
8190808_2.docx
. The masked FR4 sheet was then exposed to UV light from an ASC365
ultraviolet emitter for 6 minutes.
11. The UV light source was removed, the mask separated from the FR4
sheet, the sheet was rinsed for 5 minutes with DI water and then was placed in
an EDTA bath (15 grams of EDTA, per 1000ml of DI water) 10 minutes.
12. The FR4 sheet was removed from the EDTA bath, rinsed with DI water
for 10 minutes and then placed in an oven at 40 ºC for 5 s or until dry.
13. The FR4 sheet was placed in a bath of Shipley Electroless Cuposit 328
with 27.5% 328 (A-12.5%, L-12.5%, C-2.5%) and 72.5% zed water at 25
ºC for 5 minute intervals to record plating.
14. The copper plated FR4 sheet was then rinsed for 10 minutes and put it
into an oven at 40 ºC for 5 minutes until dry.
8190808_2.docx
CLAUSES
1. A method of forming a tive layer on a surface, sing:
activating at least a portion of a non-conductive substrate surface;
applying a magnetic field to the surface;
depositing a metal coordination complex on at least a part of the
activated portion of the surface;
removing the magnetic field;
exposing the metal coordination complex to electromagnetic radiation;
reducing the metal coordination complex to elemental metal;
removing unreduced metal coordination complex from the surface;
drying the surface; and
depositing a tive al onto the e.
2. The method of clause 1, wherein activating the substrate surface
comprises etching the surface.
3. The method of clause 2, wherein etching the surface comprises
chemical etching.
4. The method of clause 3, wherein chemical g comprises acid
g, base etching or oxidative etching.
. The method of clause 2, wherein etching the surface ses
mechanical etching.
6. The method of clause 2, wherein etching the surface comprises plasma
etching.
7. The method of clause 2, wherein etching the surface comprises laseretching.
8. The method of clause 6, wherein plasma or laser etching comprises
etching in a pre-determined pattern.
8190808_2.docx
9. The method of clause 1, where the magnetic field has a magnetic flux
density of at least 1000 gauss.
. The method of clause 9, wherein the magnetic field is onal to the
surface.
11. The method of clause 1, where depositing a metal nation complex
on at least a n of the surface comprises using a mask.
12. The method of clause 10, wherein the mask comprises an electronic
circuit.
13. The method of clause 12, wherein the electronic circuit is selected from
the group consisting of an analog t, a digital circuit, a signal circuit
and an RF circuit.
14. An analog circuit fabricated using the method of clause 1.
. A digital circuit fabricated using the method of clause 1.
16. A mixed-signal circuit fabricated using the method of clause 1.
17. An RF circuit fabricated using the method of clause 1.
18. The method of clause 1, wherein exposing the metal coordination
complex to electromagnetic radiation comprises ave radiation, infrared
radiation, visible light radiation, ultraviolet radiation, X-ray radiation or gamma
radiation.
19. The method of clause 1, where reducing the metal coordination complex
to a zero oxidation state metal comprises using a combination of metals and/or
catalysts.
. The method of clause 1, wherein removing unreduced metal
8190808_2.docx
coordination complex from the e comprises washing the surface with a
solvent.
21. The method of clause 1, wherein drying the surface comprises drying at
ambient temperature or drying at elevated temperature.
22. The method of clause 21, wherein drying the surface at ambient or
elevated temperature comprises using a vacuum chamber.
23. The method of clause 1, wherein depositing a conductive material onto
the surface comprises electrolytic deposition of a metal onto the portion of the
surface comprising the reduced metal nation complex.
24. The method of clause 23, wherein electrolytic deposition of a metal
onto the portion of the e comprising the reduced metal
coordination complex:
contacting a negative terminal of a direct current power supply with at
least the portion of the e comprising the reduced metal coordination
complex;
providing an aqueous solution comprising a salt of the metal to be
deposited, an ode made of the metal immersed in the aqueous solution or
a combination thereof;
contacting a positive terminal of the direct current power supply with the
aqueous solution;
contacting at least the portion of the surface comprising the reduced
metal coordination complex with the aqueous solution; and
turning on the power .
. The method of clause 1, wherein depositing a conductive material onto
the surface ses electroless deposition of a metal onto the portion of the
surface comprising the reduced metal coordination complex.
26. The method of clause 25, wherein olessly ting a metal onto
the portion of the surface comprising the reduced metal coordination complex
8190808_2.docx
ses contacting at least the portion of the surface sing the metal
nation complex with a solution comprising a salt of the metal, a
complexing agent and a reducing agent.
27. The method of clause 1, wherein depositing a conductive material onto
the surface comprises deposition of a non-metallic conductive substance onto
the portion of the surface comprising the d metal coordination complex.
28. The method of clause 27, wherein the tallic conductive material
is deposited onto the portion of the surface comprising the reduced metal
coordination complex by electrostatic dispersion.
29. The method of clause 1, wherein the entire non-conductive substrate
surface is activated and the metal coordination complex is deposited onto the
entire surface.
. The method of clause 1, wherein the entire non-conductive substrate
surface is activated and the metal coordination complex is deposited on a part
of the activated surface.
8190808_2.docx
Claims (20)
1. A substrate fabricated using a method comprising the steps of: activating at least a portion of a non-conductive substrate surface; depositing a metal coordination complex on a part of the activated portion of the surface; ting the metal coordination x that is located on the part of the ted portion of the e to a magnetic field to align molecules of the metal coordination complex with the magnetic field and thereby more deeply injecting the metal coordination complex into the nonconductive substrate than would occur in the step of depositing the metal coordination complex; exposing the metal coordination complex to electromagnetic radiation; reducing the metal coordination x to elemental metal; removing unreduced metal coordination complex from the surface; drying the surface; and depositing a conductive material onto the surface.
2. An analog circuit comprising the substrate ing to claim 1.
3. A digital circuit comprising the substrate according to claim 1.
4. A mixed-signal circuit comprising the substrate according to claim 1.
5. An RF t comprising the substrate according to claim 1.
6. The analog circuit according to claim 2, wherein the method further ses the step of: applying the magnetic field during the step of depositing the metal coordination complex.
7. The digital circuit according to claim 3, wherein the method further comprises the step of: applying the magnetic field during the step of depositing the metal coordination complex.
8. The mixed-signal circuit according to claim 4, n the method 8190808_2.docx further comprises the step of: applying the magnetic field during the step of depositing the metal nation complex.
9. The RF circuit according to claim 5, n the method further comprises the step of: applying the magnetic field during the step of depositing the metal coordination complex.
10. The analog circuit according to claim 2, wherein in the step of subjecting the metal nation complex to the magnetic field, ligands of the metal coordination complex are aligned with the magnetic field.
11. The digital circuit according to claim 3, wherein in the step of the subjecting the metal coordination complex to the magnetic field, ligands of the metal coordination complex are aligned with the magnetic field.
12. The mixed-signal t according to claim 4, wherein in the step of subjecting the metal nation complex to the magnetic field, ligands of the metal coordination complex are d with the magnetic field.
13. The RE circuit according to claim 5, wherein in the step of ting the metal coordination complex to the magnetic field, ligands of the metal coordination complex are aligned with the magnetic field.
14. The substrate according to claim 1, wherein the method further comprises the step of: applying the magnetic field during the step of ting the metal coordination complex.
15. The substrate according to claim 1, wherein in the step of subjecting the metal coordination complex to the magnetic field, ligands of the metal nation complex are aligned with the magnetic field.
16. The analog circuit of claim 2, the method being substantially as hereinbefore described with reference to the accompanying drawing and/or Examples. 8190808_2.docx
17. The digital circuit of claim 3, the method being substantially as hereinbefore described with reference to the accompanying drawing and/or Examples.
18. The mixed-signal circuit of claim 4, the method being substantially as hereinbefore described with reference to the accompanying drawing and/or Examples.
19. The RF circuit of claim 5, the method being substantially as hereinbefore described with nce to the accompanying drawing and/or es.
20. The substrate of claim 1, the method being substantially as before described with reference to the accompanying drawing and/or Examples. 8190808_2.docx . _ . 1 , . . . _ . .
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161525662P | 2011-08-19 | 2011-08-19 | |
US61/525,662 | 2011-08-19 | ||
US201161568736P | 2011-12-09 | 2011-12-09 | |
US61/568,736 | 2011-12-09 | ||
US13/403,797 US8784952B2 (en) | 2011-08-19 | 2012-02-23 | Method of forming a conductive image on a non-conductive surface |
US13/403,797 | 2012-02-23 | ||
NZ622408A NZ622408B2 (en) | 2011-08-19 | 2012-08-16 | Method of forming a conductive image on a non-conductive surface |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ716340A NZ716340A (en) | 2016-10-28 |
NZ716340B2 true NZ716340B2 (en) | 2017-01-31 |
Family
ID=
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