CN109203596A - 导热型聚酰亚胺基板 - Google Patents
导热型聚酰亚胺基板 Download PDFInfo
- Publication number
- CN109203596A CN109203596A CN201810208818.0A CN201810208818A CN109203596A CN 109203596 A CN109203596 A CN 109203596A CN 201810208818 A CN201810208818 A CN 201810208818A CN 109203596 A CN109203596 A CN 109203596A
- Authority
- CN
- China
- Prior art keywords
- heat
- conducting type
- polyimide substrate
- group
- conducting
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229920001721 polyimide Polymers 0.000 title claims abstract description 83
- 239000004642 Polyimide Substances 0.000 title claims abstract description 76
- 239000000758 substrate Substances 0.000 title claims abstract description 73
- 229910052751 metal Inorganic materials 0.000 claims abstract description 32
- 239000002184 metal Substances 0.000 claims abstract description 32
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000011256 inorganic filler Substances 0.000 claims abstract description 24
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 24
- 239000007787 solid Substances 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 16
- 229920005989 resin Polymers 0.000 claims abstract description 16
- 239000002245 particle Substances 0.000 claims abstract description 10
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 6
- 239000010410 layer Substances 0.000 claims description 57
- 229920002120 photoresistant polymer Polymers 0.000 claims description 56
- 229910052582 BN Inorganic materials 0.000 claims description 22
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 22
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 19
- 239000010703 silicon Substances 0.000 claims description 19
- 229910052710 silicon Inorganic materials 0.000 claims description 19
- 239000000945 filler Substances 0.000 claims description 16
- 238000011161 development Methods 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 10
- 241000282324 Felis Species 0.000 claims description 10
- 239000003431 cross linking reagent Substances 0.000 claims description 10
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
- 239000008187 granular material Substances 0.000 claims description 9
- 239000011241 protective layer Substances 0.000 claims description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 8
- 229910017083 AlN Inorganic materials 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical group [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 7
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 239000004615 ingredient Substances 0.000 claims description 7
- 239000009719 polyimide resin Substances 0.000 claims description 7
- 125000000962 organic group Chemical group 0.000 claims description 6
- 239000004925 Acrylic resin Substances 0.000 claims description 5
- 229920000178 Acrylic resin Polymers 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 150000001334 alicyclic compounds Chemical group 0.000 claims description 3
- XLTRGZZLGXNXGD-UHFFFAOYSA-N benzene;1h-pyrazole Chemical compound C=1C=NNC=1.C1=CC=CC=C1 XLTRGZZLGXNXGD-UHFFFAOYSA-N 0.000 claims description 3
- 239000002134 carbon nanofiber Substances 0.000 claims description 3
- 229910021393 carbon nanotube Inorganic materials 0.000 claims description 3
- 239000002041 carbon nanotube Substances 0.000 claims description 3
- 239000004927 clay Substances 0.000 claims description 3
- 239000004744 fabric Substances 0.000 claims description 3
- 239000000835 fiber Substances 0.000 claims description 3
- 229910021389 graphene Inorganic materials 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 3
- 239000010445 mica Substances 0.000 claims description 3
- 229910052618 mica group Inorganic materials 0.000 claims description 3
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 3
- 150000002989 phenols Chemical class 0.000 claims description 3
- -1 polydimethylsiloxane Polymers 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 238000005728 strengthening Methods 0.000 claims description 3
- 229920001187 thermosetting polymer Polymers 0.000 claims description 3
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 2
- 229920000647 polyepoxide Polymers 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
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- 230000003252 repetitive effect Effects 0.000 claims description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052725 zinc Inorganic materials 0.000 claims 1
- 239000011701 zinc Substances 0.000 claims 1
- 238000003980 solgel method Methods 0.000 abstract 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 34
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 22
- 239000010408 film Substances 0.000 description 19
- 229910000029 sodium carbonate Inorganic materials 0.000 description 17
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 7
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- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 5
- 238000000059 patterning Methods 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 229910000679 solder Inorganic materials 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 3
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 241000790917 Dioxys <bee> Species 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 238000007171 acid catalysis Methods 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000013039 cover film Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 239000012776 electronic material Substances 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 238000007761 roller coating Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- OXHNLMTVIGZXSG-UHFFFAOYSA-N 1-Methylpyrrole Chemical compound CN1C=CC=C1 OXHNLMTVIGZXSG-UHFFFAOYSA-N 0.000 description 1
- BZRAULNYWZRKMB-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3,5-diaminobenzoate Chemical compound CC(=C)C(=O)OCCOC(=O)C1=CC(N)=CC(N)=C1 BZRAULNYWZRKMB-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WYLIRYQDDKDHLT-UHFFFAOYSA-N CC1=CC=CC=C1C.CC1=CC=CC=C1C Chemical compound CC1=CC=CC=C1C.CC1=CC=CC=C1C WYLIRYQDDKDHLT-UHFFFAOYSA-N 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
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- 229910003978 SiClx Inorganic materials 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000011231 conductive filler Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000006263 metalation reaction Methods 0.000 description 1
- 238000001393 microlithography Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
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- 230000035945 sensitivity Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- B32B15/00—Layered products comprising a layer of metal
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- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1057—Polyimides containing other atoms than carbon, hydrogen, nitrogen or oxygen in the main chain
- C08G73/106—Polyimides containing other atoms than carbon, hydrogen, nitrogen or oxygen in the main chain containing silicon
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- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
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- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
- B32B27/281—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polyimides
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
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- B32B5/02—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
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- B32B9/04—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00 comprising such particular substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material
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- C—CHEMISTRY; METALLURGY
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1042—Copolyimides derived from at least two different tetracarboxylic compounds or two different diamino compounds
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1075—Partially aromatic polyimides
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/28—Nitrogen-containing compounds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08L79/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
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Abstract
本发明提供一种导热型聚酰亚胺基板,其包含至少1层绝缘层,且这些绝缘层的单面或两面上有金属层。绝缘层的材料为导热系数介于0.4‑2的导热型感光性树脂,且导热型感光性树脂包括下列成分:(a)感光性聚酰亚胺、(b)无机填充剂以及(c)二氧化硅溶液。感光性聚酰亚胺的含量占导热型感光性树脂的固体成分总重的50‑70%。无机填充剂占导热型感光性树脂固体成分总重的20‑30%,且粒径介于40nm至5μm。二氧化硅溶液包含溶胶凝胶方式聚成的二氧化硅颗粒,颗粒的粒径介于10‑15nm,且含量占该导热型感光性树脂的固体成分总重的5‑30%。
Description
技术领域
本发明揭示一种聚酰亚胺基板,特别是关于一种使用导热型感光性聚酰亚胺树脂作为绝缘层的聚酰亚胺基板。
背景技术
一般来说,聚酰亚胺树脂是由芳香族的四羧酸或其衍生物与芳香二胺、芳香二异氰酸酯缩聚而制备,制备所得的聚酰亚胺树脂具有优良的耐热性、耐化学性、机械和电特性,因而被广泛用于如半导体密封剂等绝缘耐热的电子材料。
聚酰亚胺应用于半导体元件的制程中,往往需要利用微影成像技术(MicroLithography)来制作线路图形,如果使用传统的聚酰亚胺,则必须额外加入一层光阻材料(photoresist)以进行蚀刻。因此,感光性聚酰亚胺(Photosensitive polyimide,PSPI)由于同时具有光阻及绝缘保护材料的特性,可以简化制程,使得软板电子材料制程有相当的进步,目前是相当热门的尖端材料。
然而,由于近年电路设计越趋密集,电路中所产生的热能累积,造成产品过热,成为亟欲解决的问题。目前市面上使用热传导系数较低的聚酰亚胺制作的多层基板已无法满足产业需求。
发明内容
本发明目的在于提供一种具有高导热系数同时具有良好感光性的导热型感光性树脂,以及使用其的导热型聚酰亚胺基板。
根据本发明的一个实施例,提供一种导热型聚酰亚胺基板。导热型聚酰亚胺基板包含至少1层绝缘层,且在绝缘层的单面或两面上有金属层。绝缘层的材料为导热系数介于0.4-2的导热型感光性树脂,且导热型感光性树脂包括下列成分:(a)感光性聚酰亚胺、(b)无机填充剂以及(c)二氧化硅溶液。
感光性聚酰亚胺为下式(1)的重复单元所构成的聚合物或共聚合物:
其中,m、n各自独立为10至600;X为四价有机基团,其主链部分含脂肪环基团(alicyclic compound group);Y为二价有机基团,其主链部分含硅氧烷基团(polydimethylsiloxane group);Z为二价有机基团,其支链部分至少含酚基(phenoilchydroxyl group)或羧基(carboxyl group)。此感光性聚酰亚胺的含量占导热型感光性树脂的固体成分总重的50-70%。
无机填充剂,选自氧化铝、石墨烯、无机粘土、云母粉、氮化硼、氮化铝、二氧化硅、氧化锌、氧化锆、纳米碳管及纳米碳纤维中的至少一种,此无机填充剂的含量占导热型感光性树脂固体成分总重的20-30%,且粒径介于40nm至5μm。
二氧化硅溶液,其包含溶胶凝胶方式聚成的二氧化硅颗粒,二氧化硅颗粒的粒径介于10-15nm,且含量占该导热型感光性树脂的固体成分总重的5-30%。
在一个实施例中,上述导热型感光性树脂的成分还包括含有丙烯酸树脂(acrylicresin)的光交联剂。
在一个实施例中,上述导热型感光性树脂的成分还包括热交联剂。此热交联剂包括酚类化合物、烷氧甲基胺树脂或环氧树脂。
在一个实施例中,无机填充剂为氮化硼或氮化铝。
在一个实施例中,感光性聚酰亚胺式(1)中的X为下列基团其中之一:
在一个实施例中,感光性聚酰亚胺式(1)中的Y为下列基团:
其中p=0-20。
在一个实施例中,感光性聚酰亚胺式(1)中的Z为下列基团其中之一:
在一个实施例中,二氧化硅溶液中的二氧化硅颗粒占此导热型感光性树脂固体成分总重的7.5-15%,且粒径为10-15nm。
在一个实施例中,导热型聚酰亚胺基板还具有电路元件,其位于绝缘层内并连接至少一个金属层。此电路元件包括电性连接垫、金属柱、金属连结支架或焊线。
在一个实施例中,导热型聚酰亚胺基板还包括保护层,覆盖于最外层的金属层上。保护层的材料包括感光性油墨、热固性油墨、聚对二唑苯纤维(PBO)、聚苯乙烯-苯并环丁烯共聚物(PSBCB)或感光显影覆盖膜(PIC),或可与绝缘层相同。
在一个实施例中,导热型聚酰亚胺基板为多层结构,包括两层以上的绝缘层,且每一绝缘层的单面或两面上都有金属层。
在一个实施例中,导热型聚酰亚胺基板还包括补强层,其为含浸导热型感光性树脂的碳纤维布。
为使本发明的上述内容与其他方面更能清楚易懂,下文特举实施例,并配合所附图式详细说明。然而需要特别注意的是,实施例的成分、配比、结构仅用于示例之用,并非用以限制本发明。
附图简要说明
图1绘示本发明的导热型聚酰亚胺基板的示意图;
图2A至图2F绘示图1的导热型聚酰亚胺基板的制造方法;
图3A及图3B绘示本发明的导热型聚酰亚胺基板与传统聚酰亚胺基板散热能力的比较结果,其中图3A为操作电压16V的比较结果,图3B为操作电压18V的比较结果。
具体实施方式
本发明提供一种导热型感光性树脂,其主成分为特定分子结构的感光性聚酰亚胺,并加入无机填充剂来改善导热系数,再加入二氧化硅溶液提升光穿透效应,获得具备高导热系数且感光性优良的聚酰亚胺树脂。
本发明的导热型感光性树脂,其中包含:(a)感光性聚酰亚胺;(b)无机填充剂;以及(c)二氧化硅溶液。其中(a)感光性聚酰亚胺具有下式(1)的结构:
式(1)中,m、n各自独立为10至600,X为四价有机基团,其主链部分含脂环族基团(alicyclic compound group),包含(但不限于)以下基团或其组合:
Y为二价有机基团,较佳者包含(但不限于)以下基团:
p=0-20
Y的链长以短为佳(p=0),最长可到p=20,过长将破坏感光性聚酰亚胺的性质。
Z为二价有机基团,其支链部分具有酚基(phenolic hydroxyl group)或羧基(carboxyl group),酚基或羧基的含量约占聚酰亚胺摩尔数的10-30%。调整支链酚基、羧基的含量可以控制显影的时间,当支链酚基或羧基的含量较高,则碱性显影液对感光性聚酰亚胺的溶解性较佳,可提升其显影性。
Z可包括但不限于下列基团:
(a)感光性聚酰亚胺的含量较佳地占导热型感光性树脂固体成分总重的50-80%。
本发明的导热型感光性树脂还包含(b)无机填充剂,其主要目的为增进聚酰亚胺树脂的导热性。无机填充剂可选自氧化铝、石墨烯、无机黏土、云母粉、氮化硼、二氧化硅、氮化铝、氧化锌、氧化锆、纳米碳管及纳米碳纤维中的一种或多种,且其粒径较佳介于40nm至5μm。无机填充剂的含量较佳占导热型感光性树脂固体成分总重的20-50%。
此外,本发明的导热型感光性树脂中还添加了(c)二氧化硅溶液(silicasolution,colloidal silica),其包含溶胶凝胶(Sol gel)方式聚成的纳米级二氧化硅颗粒,例如Nissan Chemical的DMAC-ST,二氧化硅颗粒粒径为10-15nm。二氧化硅溶液中的二氧化硅颗粒的含量较佳占导热型感光性树脂的固体成分总重的5-30%。本发明通过添加这两种不同粒径的填充剂,利用小粒径的二氧化硅颗粒将相对大粒径的无机填充剂隔开,使胶体内部于曝光时不至于被大粒径的无机导热填充剂遮盖,可在提升导热能力的同时,维持感光性聚酰亚胺的解析度。
本发明的导热型感光性树脂另可加入结构具有酚类化合物或烷氧甲基胺树脂的热交联剂,使聚烯亚胺分子链上的末端基在曝光烘烤时与热交联剂形成交联结构;也可加入丙烯酸树脂光交联剂,在曝光后产生酸而形成酸催化交联机制。如此产生的交联结构可增加导热型感光性树脂的耐化性及成膜性。
热交联剂其主要目的为在曝后硬烤时经由酸催化及热处理,与PI主链-OH基或末端上-OH基的邻位产生交联,使曝光区域与未曝光区域产生溶解性上的差异,进而快速形成图案。热交联剂含量约占导热型感光性树脂固体成分总重的5-40%,若低于5%,则其交联不足且不耐化学溶剂;若超过40%,则显影性较差。
光交联剂在曝光后会吸收一定波长的光能后产生自由基,引发或催化相应的单体或预聚物的聚合而形成交联。其添加量为导热型感光性树脂固体成分总重的5-40%,若低于5%,则其感光度不足;若超过40%,则显影性较差。
感光性聚酰亚胺的合成步骤为将适量的二胺单体与二酸酐单体溶于N-甲基吡咯烷酮(1-Methyl-2-pyrrolidone;NMP)中,于80℃下反应2小时,加入二甲苯(Xylene)并加热至180℃将其馏出。再加入含有酚基或羧基的二胺单体,于80℃下反应2小时,加入二甲苯并加热至180℃将其馏出,约4小时后将其冷却。导热型感光性树脂的制作方法是取上述制作完成的感光性聚酰亚胺胶体,加入无机填充剂、二氧化硅溶液、光交联剂及热交联剂即可得本发明的导热型感光性树脂(光交联剂及热交联剂可选择性加入)。
实施例1
取配备有机械搅拌器与氮气进入口的500ml三颈圆底烧瓶,加入19.88g(80毫摩尔)的1,3-双(3-氨基丙基)-1,1,3,3-四甲基二硅氧烷(1,3-Bis(3-aminopropyl)tetramethyldisiloxane)、80.7g的N-甲基吡咯烷酮(1-Methyl-2-pyrrolidone;NMP)、39.68g(160毫摩尔)的二环[2,2,2]辛-7-烯-2,3,5,6-四酸二酐(Bicyclo[2,2,2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride),将上述溶液于50-80℃反应2小时后,加入45g的二甲苯后升温至180℃后持续搅拌1.5小时,再加入21.14g(80毫摩尔)的3,5-二氨基苯甲酸2-(2-甲基丙烯酰氧基)乙基酯(2-(Methacryloyloxy)ethyl 3,5-diaminobenzoate),将上述溶液于50-80℃反应2小时后,加入50g的二甲苯后升温至180℃后持续搅拌4小时。冷却后即可得PIA-1溶液。取PIA-1溶液50g,加入11.38g的甲基丙烯酸缩水甘油酯(Glycidyl methacrylate;GMA)并于70-100℃下搅拌24小时,可得式(1)的感光性聚酰亚胺PSPI-1。
式(1)的PSPI-1中,X为Y为p=0;Z为且m=n=120。
取75g PSPI-1加入9.375g填充剂1μm氮化硼(Boron Nitride),再加入23.43g20%二氧化硅溶液(Nissan Chemical的DMAC-ST,其二氧化硅颗粒粒径为10-15nm)均匀混合,可得导热型感光性树脂PSPI-BN1。利用线棒涂布PSPI-BN1于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
实施例2
将实施例1中的PSPI-1溶液加入12.5g填充剂1μm氮化硼(Boron Nitride),再加入25g 20%二氧化硅溶液(颗粒粒径为10-15nm)均匀混合,可得导热型感光性树脂PSPI-BN2。利用线棒涂布PSPI-BN2于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
实施例3
将实施例1中的PSPI-1溶液加入16.07g填充剂1μm氮化硼(Boron Nitride),再加入26.78g 20%二氧化硅溶液(颗粒粒径为10-15nm)均匀混合,可得导热型感光性树脂PSPI-BN3。利用线棒涂布PSPI-BN3于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
实施例4
将实施例1中的PSPI-1溶液加入16.07g填充剂50nm氮化硼(Boron Nitride),再加入26.78g 20%二氧化硅溶液(颗粒粒径为10-15nm)均匀混合,可得导热型感光性树脂PSPI-BN4。利用线棒涂布PSPI-BN4于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
实施例5
将实施例1中的PSPI-1溶液加入12.5g填充剂5μm氮化铝(Aluminium Nitride),再加入25g 20%二氧化硅溶液(颗粒粒径为10-15nm)均匀混合,可得导热型感光性树脂PSPI-BN5。利用线棒涂布PSPI-BN2于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
比较例1
将实施例1中的PSPI-1溶液加入9.375g填充剂1μm氮化硼(Boron Nitride)均匀混合,可得导热型感光性树脂PSPI-CT1。利用线棒涂布PSPI-CT1于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
比较例2
将实施例1中的PSPI-1溶液加入12.5g填充剂1μm氮化硼(Boron Nitride)均匀混合,可得导热型感光性树脂PSPI-CT2。利用线棒涂布PSPI-CT2于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
比较例3
将实施例1中的PSPI-1溶液加入16.07g填充剂1μm氮化硼(Boron Nitride)均匀混合,可得导热型感光性树脂PSPI-CT3。利用线棒涂布PSPI-CT3于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
比较例4
将实施例1中的PSPI-1溶液加入16.07g填充剂50nm氮化硼(Boron Nitride)均匀混合,可得导热型感光性树脂PSPI-CT4。利用线棒涂布PSPI-CT4于基材上,经90℃烘箱下,8分钟的预烤程序后,可得膜厚约15μm的薄膜,并以曝光机(功率7kw)投以约400mJ/cm2的能量加以曝光,再以1wt%(重量百分比)碳酸钠(Sodium carbonate)显影剂加以显影,显影时间为1分钟。接着在氮气烘箱200℃下进行2小时的硬烤程序,便可得到耐热性的显影图形。
实施例1-5和比较例1-4的导热型感光性树脂其配方及特性如表一所示:
表一导热型感光性树脂特性测量与比较
*解析度表示可达到且可重复的最小图案尺寸,数值越小越佳
*占比皆指占导热型感光树脂的「固体含量」的重量百分比
表一中,填充剂占比是指无机填充剂重量占导热型感光树脂的固体含量的百分比,计算公式如下:
%填充剂=(W填充剂/Wsolid)×100%
固体含量(%solid)测量方法为,取适当重量胶体,秤重后使用200℃烘烤90分钟,烘烤后再次秤重得固体重量(Wsolid)。得知固体重量后,固体含量可由以下公式计算而得:
%solid=(Wsolid/Wtotal)×100%
以实施例2的导热型感光树脂PSPI-BN2为例,其为聚酰亚胺PSPI-1 75g(固体含量50%)添加12.5g无机填充剂氮化硼,因此
本发明的导热型感光树脂组成物实施例1-4,为相同的感光性聚酰亚胺加入不同重量百分比(wt%)的无机填充剂,且添加相同重量百分比的纳米级二氧化硅颗粒(以二氧化硅溶液方式添加)。相对的,比较例1-4为相同的感光性聚酰亚胺加入不同重量百分比(wt%)的无机填充剂,但未添加二氧化硅溶液。由表一可知,加入二氧化硅溶液,具有不同粒径的填充剂的实施例1-4,比起仅加入单一一种无机填充剂的比较例1-4,其导热系数、热阻(热阻越小越好)与解析度表现(解析度越小越好)都较佳。更甚者,虽然比较例3的主成分也是感光性聚酰亚胺,但由于仅添加一种无机填充剂,且添加比例过高,导致根本无法显影。另外,比较例3虽然使用了粒径较小(50nm)的无机填充剂,但由于添加比例过高,且未添加二氧化硅溶液,仍然无法显影,且导热系数与热阻都较差。实施例5使用另外一种无机填充剂(氮化铝)与二氧化硅溶液混合,同样能够获得高导热、低热阻、解析度优良的效果。本发明通过添加较大粒径的无机填充剂,以及粒径较小的二氧化硅溶液,利用小粒径的二氧化硅颗粒将相对大粒径的无机填充剂隔开,使胶体内部于曝光时不至于被大粒径的无机导热填充剂遮盖,可获得具备高导热系数且感光性优良的导热型感光性树脂。
导热型聚酰亚胺基板
本发明导热型感光性树脂由于兼具导热效果良好以及高感光性的优点,可有多种用途。例如可以作为薄型化基板、载板的介电材料,用以制作多层的叠构基板。
图1为本发明的导热型聚酰亚胺的示意图。导热型聚酰亚胺基板100的结构包括基材10、金属层20,40、电路元件21、绝缘层30以及保护层50。导热型聚酰亚胺基板100可作为半导体元件的载板,通过锡铅凸块60(solder bump)连结半导体IC 70。
以下通过图2A至图2F说明导热型聚酰亚胺基板100的制造方式。首先如图1所示,提供基材10。基材10的材料可包括BT树脂基板、FR-4基板、FR-5基板、ABF树脂基板或FCCL软性铜箔基板等,也可为含浸导热型感光性树脂的碳纤维布,作为加强导热型聚酰亚胺基板强度的补强层。本发明并不对此限制。基材10的上下都具有金属层20,其材质可为铜或其他导电材料。
接着如图2B所示,图案化(patterning)上下金属层20,形成电路设计所需的样式。图案化的方式可为皆知的黄光微影制程,本发明并不限制。
在一个实施例中,如图2C所示,图案化的金属层20上可放置电路元件21,其可为被动元件、主动元件、电性连接垫、金属柱、金属连结支架或焊线等。
接着,如图2D所示,于基材10及金属层20上形成绝缘层30。绝缘层的材料即为前述的导热型感光性树脂,其可直接曝光显影,而不需要额外使用光阻材料来图案化,且具有高导热性,可降低基板的温度。绝缘层30可用印刷、旋涂、辊涂(roller coating)或压贴合(laminating)等方式形成,并使用UV光曝光,再以显影剂去除的方式进行图案化形成通孔31。
然后,如图2E所示,在绝缘层30上形成另外一层图案化金属层40。图案化金属层较佳的制作方法是先对绝缘层30与通孔31进行表面金属化,形成薄金属层使其成为后续制程的金属形成基底,并增加附着力。然后再以电镀的方式于特定地方加厚金属,形成电路设计所需样式的图案化金属层40。
最后,如图2F所示,在最外层的金属层20、40上形成保护层50,图案化使内部的金属层外露,再将金属层外露的部分与半导体IC 70电性连接,便完成图1所示导热型聚酰亚胺基板100。图2F中所示的金属电性连接的方式为覆晶(Flip Chip)与锡铅凸块60(SolderBump),然而也可采用如打线连结(wire bonding)等的其他方式,本发明并不限制。保护层50的材料可与绝缘层30相同,使用本发明的导热型感光性树脂,也可使用感光性油墨、热固性油墨、聚对二唑苯纤维(PBO)、聚苯乙烯-苯并环丁烯共聚物(PSBCB)或感光显影覆盖膜(PIC)。
图1的导热型聚酰亚胺基板100包括2层金属层20、40,于其他实施例中,可重复图2D至图2F的增层结构制程,便可制作出更多层数的导热型聚酰亚胺基板。
另外,本发明的导热型聚酰亚胺基板并不限定必须依上述制程制造,也可使用其他皆知的半导体制程。只要复数金属层之间的绝缘层使用本发明所述的导热型感光性树脂,都属于本发明的范围。
图3A及图3B比较传统聚酰亚胺基板与本发明导热型聚酰亚胺基板的散热能力。其将相同的发热元件分别设置在传统PSPI基板(单纯使用PSPI作为绝缘层),以及使用本发明的导热型感光性树脂作为绝缘层的基板中,再用红外线温度扫描仪测量基板的工作温度。图中使用了本发明实施例3、5以及比较例4的导热型感光性树脂,图3A为操作电压16V的测试结果,图3B为操作电压18V的测试结果。由图可知,使用单一填充剂的聚酰亚胺基板(比较例2,导热系数0.19),其散热效果较一般的PSPI基板(导热系数约0.1-0.2)好,但并没有很明显的差异。而使用本发明的导热型感光性树脂(实施例3、5)的导热型聚酰亚胺基板,其工作温度跟传统聚酰亚胺基板相比较有极大差异,当操作电压较高时,差异更为明显,甚至降低达40%之多(90℃至55℃)。
本发明的导热型聚酰亚胺基板,由于使用了导热型感光性树脂,其工作温度比起传统的PSPI基板(导热系数0.1-0.2)大幅降低,且由于仍保有感光性,图案化制程时不需要额外使用光阻,可简化制程、增加良率。
虽然本发明以实施例说明如上,但这些实施例并非用以限制本发明。本领域的通常知识者在不脱离本发明技艺精神的范畴内,当可对这些实施例进行等效实施或变更,故本发明的保护范围应以其后所附的权利要求范围为准。
【符号说明】
100:导热型聚酰亚胺基板
10:基材
20、40:金属层
21:电路元件
30:绝缘层
31:通孔
50:保护层
60:凸块
70:半导体IC。
Claims (15)
1.一种导热型聚酰亚胺基板,包含:
至少一层绝缘层,且在这些绝缘层的单面或两面上有金属层;
该绝缘层的材料为导热系数介于0.4-2的导热型感光性树脂,且该导热型感光性树脂包括下列成分:
(a)感光性聚酰亚胺,其为下式(1)的重复单元所构成的聚合物或共聚合物:
其中,m、n各自独立为10至600;X为四价有机基团,其主链部分含脂肪环基团(alicyclic compound group);Y为二价有机基团,其主链部分含硅氧烷基团(polydimethylsiloxane group);Z为二价有机基团,其支链部分至少含酚基(phenoilchydroxyl group)或羧基(carboxyl group),该感光性聚酰亚胺的含量占该导热型感光性树脂的固体成分总重的50-70%;
(b)无机填充剂,选自氧化铝、石墨烯、无机粘土、云母粉、氮化硼、氮化铝、二氧化硅、氧化锌、氧化锆、纳米碳管及纳米碳纤维中的至少一种,该无机填充剂的含量占该导热型感光性树脂固体成分总重的20-30%,且粒径介于40nm至5μm;以及
(c)二氧化硅溶液,其包含溶胶凝胶方式聚成的二氧化硅颗粒,这些二氧化硅颗粒的粒径介于10-15nm,且这些二氧化硅颗粒含量占该导热型感光性树脂的固体成分总重的5-30%。
2.如权利要求1所述的导热型聚酰亚胺基板,其中该导热型感光性树脂的成分还包括含丙烯酸树脂(acrylic resin)的光交联剂。
3.如权利要求1所述的导热型聚酰亚胺基板,其中该导热型感光性树脂的成分还包括热交联剂,该热交联剂包括酚类化合物、烷氧甲基胺树脂或环氧树脂。
4.如权利要求1所述的导热型聚酰亚胺基板,其中该导热型感光性树脂中的该无机填充剂为氮化硼或氮化铝。
5.如权利要求1所述的导热型聚酰亚胺基板,其中该导热型感光性树脂中的X为下列基团其中之一:
6.如权利要求1所述的导热型聚酰亚胺基板,其中该导热型感光性树脂中的Y为下列基团:
其中p=0-20。
7.如权利要求1所述的导热型聚酰亚胺基板,其中该导热型感光性树脂中的Z为下列基团其中之一:
8.如权利要求1所述的导热型聚酰亚胺基板,其中该导热型感光性树脂内的这些二氧化硅颗粒占该导热型感光性树脂固体成分总重的7.5-15%,且粒径为10-15nm。
9.如权利要求1所述的导热型聚酰亚胺基板,还包括电路元件,其位于绝缘层内并连接至少一个该金属层。
10.如权利要求9所述的导热型聚酰亚胺基板,其中该电路元件包括电性连接垫、金属柱、金属连结支架或焊线。
11.如权利要求1所述的导热型聚酰亚胺基板,还包括保护层,该保护层覆盖于最外层的该金属层上。
12.如权利要求11所述的导热型聚酰亚胺基板,其中该保护层的材料包括感光性油墨、热固性油墨、聚对二唑苯纤维(PBO)、聚苯乙烯-苯并环丁烯共聚物(PSBCB)或感光显影覆盖膜(PIC)。
13.如权利要求11所述的导热型聚酰亚胺基板,其中该保护层的材料与该绝缘层相同。
14.如权利要求1所述的导热型聚酰亚胺基板,其中包括两层以上的绝缘层,且每一绝缘层的单面或两面上都有金属层。
15.如权利要求1所述的导热型聚酰亚胺基板,其还包括补强层,该补强层为含浸该导热型感光性树脂的碳纤维布。
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