JP2013139543A - 電解質材料調製物、電解質材料調製物より形成された電解質材料ポリマー及びその使用 - Google Patents
電解質材料調製物、電解質材料調製物より形成された電解質材料ポリマー及びその使用 Download PDFInfo
- Publication number
- JP2013139543A JP2013139543A JP2012142849A JP2012142849A JP2013139543A JP 2013139543 A JP2013139543 A JP 2013139543A JP 2012142849 A JP2012142849 A JP 2012142849A JP 2012142849 A JP2012142849 A JP 2012142849A JP 2013139543 A JP2013139543 A JP 2013139543A
- Authority
- JP
- Japan
- Prior art keywords
- monomer
- electrolyte material
- material preparation
- solid state
- polymer
- 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.)
- Pending
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 38
- 239000000463 material Substances 0.000 title abstract description 6
- 238000009472 formulation Methods 0.000 title abstract 3
- 239000000203 mixture Substances 0.000 title abstract 3
- 239000003990 capacitor Substances 0.000 claims abstract description 83
- 239000000178 monomer Substances 0.000 claims abstract description 61
- 239000007787 solid Substances 0.000 claims abstract description 59
- 239000002001 electrolyte material Substances 0.000 claims description 60
- 238000002360 preparation method Methods 0.000 claims description 58
- 125000004432 carbon atom Chemical group C* 0.000 claims description 23
- 239000007800 oxidant agent Substances 0.000 claims description 20
- 239000003792 electrolyte Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 7
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- 150000002978 peroxides Chemical class 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000011888 foil Substances 0.000 description 29
- NOZWWNARZBMOQB-UHFFFAOYSA-K C(C)O.C1(=CC=C(C=C1)S(=O)(=O)[O-])C.[Fe+3].C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C1(=CC=C(C=C1)S(=O)(=O)[O-])C Chemical compound C(C)O.C1(=CC=C(C=C1)S(=O)(=O)[O-])C.[Fe+3].C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C1(=CC=C(C=C1)S(=O)(=O)[O-])C NOZWWNARZBMOQB-UHFFFAOYSA-K 0.000 description 22
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 17
- 229910052782 aluminium Inorganic materials 0.000 description 16
- 230000001590 oxidative effect Effects 0.000 description 15
- 238000006116 polymerization reaction Methods 0.000 description 14
- 229920001940 conductive polymer Polymers 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 8
- GKWLILHTTGWKLQ-UHFFFAOYSA-N 2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=CSC=C21 GKWLILHTTGWKLQ-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 0 *C1(*)OC2=CSCC2O1 Chemical compound *C1(*)OC2=CSCC2O1 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- -1 methylene, ethylene, propylene Chemical group 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000014509 gene expression Effects 0.000 description 4
- FYMCOOOLDFPFPN-UHFFFAOYSA-K iron(3+);4-methylbenzenesulfonate Chemical compound [Fe+3].CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1 FYMCOOOLDFPFPN-UHFFFAOYSA-K 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000011244 liquid electrolyte Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920000767 polyaniline Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QTTXPSXLMFARIT-UHFFFAOYSA-N COc1c[nH]cc1OC Chemical compound COc1c[nH]cc1OC QTTXPSXLMFARIT-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 description 2
- AVBCFBRGFCGJKX-UHFFFAOYSA-N thieno[3,4-d][1,3]dioxole Chemical compound S1C=C2OCOC2=C1 AVBCFBRGFCGJKX-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 description 1
- ZPNBZMUFFHCECY-UHFFFAOYSA-N 3-methyl-3,4-dihydro-2h-thieno[3,4-b][1,4]dioxepine Chemical compound O1CC(C)COC2=CSC=C21 ZPNBZMUFFHCECY-UHFFFAOYSA-N 0.000 description 1
- RATGTOHXIKANMQ-UHFFFAOYSA-N CC1COc2c[nH]cc2OC1 Chemical compound CC1COc2c[nH]cc2OC1 RATGTOHXIKANMQ-UHFFFAOYSA-N 0.000 description 1
- ZUDCKLVMBAXBIF-UHFFFAOYSA-N COc1c[s]cc1OC Chemical compound COc1c[s]cc1OC ZUDCKLVMBAXBIF-UHFFFAOYSA-N 0.000 description 1
- QMHIMXFNBOYPND-UHFFFAOYSA-N Cc1c[s]cn1 Chemical compound Cc1c[s]cn1 QMHIMXFNBOYPND-UHFFFAOYSA-N 0.000 description 1
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical class [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 229910013684 LiClO 4 Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- VBIXEXWLHSRNKB-UHFFFAOYSA-N ammonium oxalate Chemical compound [NH4+].[NH4+].[O-]C(=O)C([O-])=O VBIXEXWLHSRNKB-UHFFFAOYSA-N 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 125000005046 dihydronaphthyl group Chemical group 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- FCZCIXQGZOUIDN-UHFFFAOYSA-N ethyl 2-diethoxyphosphinothioyloxyacetate Chemical compound CCOC(=O)COP(=S)(OCC)OCC FCZCIXQGZOUIDN-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000002608 ionic liquid Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910001251 solid state electrolyte alloy Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Images
Classifications
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/124—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one nitrogen atom in the ring
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/126—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one sulfur atom in the ring
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/0029—Processes of manufacture
- H01G9/0036—Formation of the solid electrolyte layer
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/022—Electrolytes; Absorbents
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/022—Electrolytes; Absorbents
- H01G9/025—Solid electrolytes
- H01G9/028—Organic semiconducting electrolytes, e.g. TCNQ
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/15—Solid electrolytic capacitors
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/10—Definition of the polymer structure
- C08G2261/14—Side-groups
- C08G2261/142—Side-chains containing oxygen
- C08G2261/1424—Side-chains containing oxygen containing ether groups, including alkoxy
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3221—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more nitrogen atoms as the only heteroatom, e.g. pyrrole, pyridine or triazole
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3222—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more oxygen atoms as the only heteroatom, e.g. furan
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3223—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3228—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing nitrogen and oxygen as heteroatoms
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3229—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing nitrogen and sulfur as heteroatoms
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Power Engineering (AREA)
- Electrochemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Conductive Materials (AREA)
Abstract
Description
(a)化学式(I)のモノマー
(b)化学式(II)のモノマー
Aは、(Rx)pで置換された炭素数1から4のアルキレン基であり;
Xは、O又はSであり;
B1は、O、S、又はNであり;
B2は、N又はCであり;
R1、R2、R3、及びRXは独立して、H、置換又は非置換の炭素数1から20のアルキル又はアルコキシ、置換又は非置換の炭素数6から20のアリールであり;
pは、0から2の範囲の整数であり;及び
q及びwは独立して、0又は1の整数であり、
モノマー(b)の量は、モノマー(a)の100重量部に基づき、約1重量部から約800重量部である、
ことを特徴とする電解質材料調製物を提供することである。
固体状態コンデンサ1−21及び比較例固体状態コンデンサ22を、下記の方法に従って電解質材料調製物1−21及び比較例電解質材料調製物22を各々用いて調製した。図1に示されるコンデンサ部品1を、5分間選択された電解質材料調製物に含浸させ、その後、含浸させたコンデンサ部品1を該調製物から取り出し、重合がなされるように約25℃から約260℃の温度に加熱し、含浸させたコンデンサ部品1において固体状態電解質を形成させた。固体状態電解質の粒子径分布(スパン値)を測定し、その結果を表1で一覧とした。次に、固体状態電解質を含有するコンデンサ部品1を箱の底部に置き、箱を露出されたワイヤで密封し、固体状態コンデンサを得た。調製された固体状態コンデンサの特性を各々測定し、結果を表1で一覧とした。測定機器及び方法は、下記の通りである。
固体状態コンデンサのキャパシタンスを、20℃及び120HzでHP4284A LCRの計測器で測定した。
固体状態コンデンサの耐電圧を、Chroma Model 11200のコンデンサ漏電電流/絶縁抵抗計を用いて測定した。
固体状態コンデンサの固体状態電解質のスパン値を、HORIBA LA−950V2レーザー粒子径アナライザーを用いて測定した。
本出願は、台湾特許出願100150085(出願日2011年12月30日)に基づく優先権を主張しており、その内容は本明細書に参照として取り込まれる。
Claims (10)
- (a)化学式(I)のモノマー
(b)化学式(II)のモノマー
Aは、(Rx)pで置換された炭素数1から4のアルキレン基であり;
Xは、O又はSであり;
B1は、O、S、又はNであり;
B2は、N又はCであり;
R1、R2、R3、及びRXは独立して、H、置換若しくは非置換の炭素数1から20のアルキル若しくはアルコキシ、又は置換若しくは非置換の炭素数6から20のアリールであり;
pは、0から2の範囲の整数であり;
q及びwは独立して、0又は1の整数であり、
モノマー(b)の量は、モノマー(a)の100重量部に基づき、約1重量部から約800重量部である、
ことを特徴とする電解質材料調製物。 - アルカリ金属過硫酸塩、アンモニウム塩、ペルオキシド、有機酸の鉄酸、1又は2以上の有機基を含む無機酸、及びこれらの組み合わせからなる群より選択される酸化剤をさらに含む、請求項1に記載の電解質材料調製物。
- 酸化剤の量は、モノマー(a)とモノマー(b)との全量の100重量部につき、約5重量部から約3000重量部である、
ことを特徴とする請求項4に記載の電解質材料調製物。 - 請求項1乃至5のいずれか1項に記載の電解質材料調製物を重合することにより得られる電解質材料として有用なポリマー。
- ポリマーの分子量は、約1,000から約500,000の範囲である、
ことを特徴とする請求項6に記載のポリマー。 - ポリマーの平均粒子径は、約10nmから約500nmの範囲である、
ことを特徴とする請求項6に記載のポリマー。 - ポリマーのスパン値は、約0.1から約2の範囲である、
ことを特徴とする請求項6に記載のポリマー。 - 陽極と、
陽極上に形成された誘電体層と、
陰極と、
誘電体層と陰極との間の固体状態電解質と、
を含む固体状態コンデンサであって、
固体状態電解質は、請求項6乃至9のいずれか1項に記載のポリマーである、
ことを特徴とする固体状態コンデンサ。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW100150085A TWI464934B (zh) | 2011-12-30 | 2011-12-30 | 電解質材料調配物、由此形成之電解質材料聚合物及其用途 |
TW100150085 | 2011-12-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2013139543A true JP2013139543A (ja) | 2013-07-18 |
Family
ID=46656608
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012142849A Pending JP2013139543A (ja) | 2011-12-30 | 2012-06-26 | 電解質材料調製物、電解質材料調製物より形成された電解質材料ポリマー及びその使用 |
Country Status (6)
Country | Link |
---|---|
US (1) | US9036333B2 (ja) |
JP (1) | JP2013139543A (ja) |
KR (1) | KR101499289B1 (ja) |
CN (1) | CN102643518B (ja) |
DE (1) | DE102012209633A1 (ja) |
TW (1) | TWI464934B (ja) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI532783B (zh) * | 2013-05-20 | 2016-05-11 | 長興材料工業股份有限公司 | 導電性材料調配物及其用途 |
CN110517893A (zh) * | 2019-08-14 | 2019-11-29 | 湖南艾华集团股份有限公司 | 一种耐高压的固态铝电解电容器及其制备方法 |
CN113972072B (zh) * | 2021-11-05 | 2023-04-07 | 肇庆绿宝石电子科技股份有限公司 | 一种16v固态电容器及其制造方法 |
EP4279524A1 (en) | 2022-05-20 | 2023-11-22 | Agfa-Gevaert Nv | Novel polythiophene/polyanion compositions |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04108825A (ja) * | 1990-08-28 | 1992-04-09 | Matsushita Electric Ind Co Ltd | コンデンサ |
JP2003261573A (ja) * | 2001-12-27 | 2003-09-19 | Bayer Ag | 中性ポリチオフェンの製造方法、そのような化合物、中性コポリマー、および中性化合物およびコポリマーの使用 |
JP2004277736A (ja) * | 2003-02-28 | 2004-10-07 | Kyoto Univ | 導電性重合体及びその製造方法並びにそれを用いた有機太陽電池 |
JP2005120363A (ja) * | 2003-09-25 | 2005-05-12 | Showa Denko Kk | π共役系共重合体、その製造方法及びその共重合体を用いたコンデンサ |
WO2010007648A1 (ja) * | 2008-07-16 | 2010-01-21 | ナガセケムテックス株式会社 | 新規複素環式芳香族化合物及びポリマー |
JP2011228636A (ja) * | 2010-04-01 | 2011-11-10 | Japan Carlit Co Ltd | 固体電解コンデンサ及びその製造方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4609971A (en) | 1983-08-11 | 1986-09-02 | North American Philips Corporation | Electrolytic capacitor with polymer conductor |
DE3636100A1 (de) | 1986-10-23 | 1988-05-05 | Roederstein Kondensatoren | Festkoerperkondensator mit einem elektrisch leitfaehigen polymeren als bestandteil des festelektrolyten |
DE3814730A1 (de) | 1988-04-30 | 1989-11-09 | Bayer Ag | Feststoff-elektrolyte und diese enthaltende elektrolyt-kondensatoren |
EP1501107B1 (en) | 2002-03-28 | 2013-01-09 | Nippon Chemi-Con Corporation | Solid electrolytic capacitor and process for producing the same |
JP4508913B2 (ja) * | 2005-03-23 | 2010-07-21 | 三洋電機株式会社 | 固体電解コンデンサ及び固体電解コンデンサ用陽極材料の製造方法 |
DE102005028262B4 (de) * | 2005-06-17 | 2010-05-06 | Kemet Electronics Corp. | Kondensator mit einer Elektrode und Herstellungsverfahren für den Kondensator mit der Elektrode |
KR101927676B1 (ko) | 2009-12-18 | 2018-12-10 | 닛산 가가쿠 가부시키가이샤 | 3,4-디알콕시티오펜 공중합체, 및 그의 제조 방법 및 소자 |
-
2011
- 2011-12-30 TW TW100150085A patent/TWI464934B/zh active
-
2012
- 2012-05-15 CN CN201210151759.0A patent/CN102643518B/zh active Active
- 2012-05-23 US US13/478,997 patent/US9036333B2/en active Active
- 2012-06-08 DE DE102012209633A patent/DE102012209633A1/de not_active Ceased
- 2012-06-20 KR KR1020120066090A patent/KR101499289B1/ko active IP Right Grant
- 2012-06-26 JP JP2012142849A patent/JP2013139543A/ja active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04108825A (ja) * | 1990-08-28 | 1992-04-09 | Matsushita Electric Ind Co Ltd | コンデンサ |
JP2003261573A (ja) * | 2001-12-27 | 2003-09-19 | Bayer Ag | 中性ポリチオフェンの製造方法、そのような化合物、中性コポリマー、および中性化合物およびコポリマーの使用 |
JP2010018628A (ja) * | 2001-12-27 | 2010-01-28 | Hc Starck Gmbh | 中性化合物の使用 |
JP2004277736A (ja) * | 2003-02-28 | 2004-10-07 | Kyoto Univ | 導電性重合体及びその製造方法並びにそれを用いた有機太陽電池 |
JP2005120363A (ja) * | 2003-09-25 | 2005-05-12 | Showa Denko Kk | π共役系共重合体、その製造方法及びその共重合体を用いたコンデンサ |
WO2010007648A1 (ja) * | 2008-07-16 | 2010-01-21 | ナガセケムテックス株式会社 | 新規複素環式芳香族化合物及びポリマー |
JP2011228636A (ja) * | 2010-04-01 | 2011-11-10 | Japan Carlit Co Ltd | 固体電解コンデンサ及びその製造方法 |
Also Published As
Publication number | Publication date |
---|---|
DE102012209633A1 (de) | 2013-07-04 |
CN102643518A (zh) | 2012-08-22 |
TWI464934B (zh) | 2014-12-11 |
US20130170102A1 (en) | 2013-07-04 |
KR101499289B1 (ko) | 2015-03-05 |
TW201327973A (zh) | 2013-07-01 |
DE102012209633A8 (de) | 2013-09-26 |
KR20130079101A (ko) | 2013-07-10 |
CN102643518B (zh) | 2016-08-10 |
US9036333B2 (en) | 2015-05-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5777667B2 (ja) | 導電性ポリマー複合体並びにその調製及びその使用 | |
JP5745881B2 (ja) | 固体電解コンデンサ | |
JP5968485B2 (ja) | 電解質材料配合物、該電解質材料配合物から形成される電解質材料組成物およびその使用 | |
JP2013139543A (ja) | 電解質材料調製物、電解質材料調製物より形成された電解質材料ポリマー及びその使用 | |
WO2012053474A1 (ja) | 導電性組成物及び導電性被膜の製造方法 | |
US10504658B2 (en) | Conductive material formulation and use thereof | |
JP2005116777A (ja) | 固体電解コンデンサ | |
JP2014037504A (ja) | 導電性組成物及び導電性被膜 | |
JP5656127B2 (ja) | 電解質材料配合物、それから形成される電解質材料組成物、及びその使用 | |
JP2014037508A (ja) | 導電性組成物及び導電性被膜 | |
JP2012077218A (ja) | 重合性モノマー組成物、固体電解コンデンサの製造方法 | |
JP7072686B2 (ja) | 導電性ポリマー材料及びその使用 | |
JP5645152B2 (ja) | 固体電解コンデンサ及びその製造方法 | |
JP5481639B2 (ja) | 導電性高分子製造用酸化剤とそれを用いた固体電解コンデンサ及びその製造方法 | |
JP2013179292A (ja) | 導電性高分子製造用酸化剤溶液及びそれを用いた固体電解コンデンサの製造方法 | |
JP2008091589A (ja) | 固体電解質、固体電解コンデンサ、及びその製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20131028 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20131112 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20140106 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20140109 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140512 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20141028 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20150128 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20150407 |