Conductive polymer composition with a dual crosslinker system for capacitors
View Patent ↗A capacitor with improved electronic properties is described. The capacitor has an anode, a dielectric on said anode and a cathode on the dielectric. The cathode has a conductive polymer defined as —(CR 1 R 2 CR 3 R 4 —) x — wherein at least one of R 1 , R 2 , R 3 or R 4 comprises a group selected from thiophene, pyrrole or aniline with the proviso that none of R 1 , R 2 , R 3 or R 4 contain —SOOH or COOH; a organofunctional silane; and an organic compound with at least two functional groups selected from the group consisting of carboxylic acid and epoxy.
1. A capacitor comprising:
an anode;
a dielectric on said anode;
a cathode on said dielectric wherein said cathode comprises:
a first layer closest to said dielectric comprising poly(3,4-ethylenedioxythiophene) and a toluene sulphonate; and
a second layer comprising a conductive polymer comprising repeating units of —(CR 1 R 2 CR 3 R 4 ) wherein at least one of R 1 , R 2 , R 3 or R 4 comprises a group selected from thiophene, pyrrole or aniline with the proviso that none of R 1 , R 2 , R 3 or R 4 contain SOON or COOH;
0.0005 to 0.1000 grams of an organofunctional silane per gram of said conductive polymer; and
0.001 to 0.100 grams of an organic compound per gram of said conductive polymer with at least two functional groups selected from the group consisting of carboxylic acid and epoxy.
2. The capacitor of claim 1 wherein said cathode further comprises a polyanion.
3. The capacitor of claim 2 wherein said polyanion is polystyrene sulfonic acid.
4. The capacitor of claim 1 wherein said conductive polymer comprises a polythiophene.
5. The capacitor of claim 4 wherein said conductive polymer is poly(3,4-ethylenedioxythiophene).
6. The capacitor of claim 1 wherein said organofunctional silane is a glycidyl silane.
7. The capacitor of claim 6 wherein said glycidyl silane is defined by the formula:
wherein R 1 is an alkyl of 1 to 14 carbons; and
each R 2 is independently an alkyl of 1 to 6 carbons.
8. The capacitor of claim 7 wherein said R 1 is selected from the group consisting of methyl, ethyl and propyl.
9. The capacitor of claim 7 wherein said glycidyl silane is defined by the formula:
10. The capacitor of claim 1 wherein said organofunctional silane is defined by the formula:
XR 1 Si(R 3 ) 3-n (R 2 ) n
wherein X is an organic functional group selected from the group consisting of amino, epoxy, anhydride, hydroxy, mercapto, sulfonate, carboxylate, phosphonate, halogen, vinyl, methacryloxy, ester and alkyl;
R 1 is an aryl or (CH 2 ) m wherein m can be 0 to 14;
R 2 is individually a hydrolysable functional group;
R 3 is individually an alkyl functional group of 1-6 carbons; and
n is 1 to 3.
11. The capacitor of claim 10 wherein said hydrolysable functional group is selected from the group consisting of alkoxy, acyloxy, halogen and amine.
12. The capacitor of claim 1 wherein said organofunctional silane is defined by the formula:
Y(Si(R 3 ) 3-n (R 2 ) n ) 2
wherein Y is any organic moiety that contains reactive or nonreactive functional groups such as alkyl, aryl, sulfide or melamine;
R 2 is individually a hydrolysable functional group;
R 3 is individually an alkyl functional group of 1-6 carbons; and
n is 1 to 3.
13. The capacitor of claim 1 wherein said organofunctional silane is selected from the group consisting of: 3-glycidoxypropyltrimethoxysilane, 3-aminopropytriethoxysilane, aminopropylsilanetriol, (triethoxysilyl)propylsuccinic anhydride, 3-mercaptoprpyltrimethoxysilane, vinyltrimethoxysilane, 3-metacryloxypropyltrimethoxysilane, 3-trihydroxysilyl-1-propane sulfonic acid and octyltriethyoxysilane.
14. The capacitor of claim 1 wherein said organic compound is an epoxy crosslinking compound.
15. The capacitor of claim 14 wherein said epoxy crosslinking compound is defined by the formula:
wherein the X is an alkyl or substituted alkyl of 0-14 carbons, an aryl or substituted aryl, an ethylene ether or substituted ethylene ether, polyethylene ether or substituted polyethylene ether with 2-20 ethylene ether groups or combinations thereof.
16. The capacitor of claim 15 wherein said substitute is an epoxy group.
17. The capacitor of claim 15 wherein alkyl or substituted alkyl has 0-6 carbons.
18. The capacitor of claim 15 wherein said epoxy crosslinking compound is selected from the group consisting of: ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, 1,4-butanediol diglycidyl ether, pentylene glycol diglycidyl ether, hexylene glycol diglycidyl ether, cyclohexane dimethanol diglycidyl ether, resorcinol glycidyl ether, glycerol diglycidyl ether, glycerol polyglycidyl ethers, diglycerol polyglycidyl ethers, trimethylolpropane polyglycidyl ethers, sorbitol diglycidyl ether, sorbitol polyglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, polytetramethylene glycol diglycidyl ether, di(2,3-epoxypropyl) ether, 1,3-butadiene diepoxide, 1,5-hexadiene diepoxide, 1,2,7,8-diepoxyoctane, 1,2,5,6-Diepoxycyclooctane, 4-vinyl cyclohexene diepoxide, bisphenol diglycidyl ether and a maleimide-epoxy compound.
19. The capacitor of claim 14 wherein said epoxy crosslinking compound is a glycidyl ether.
20. The capacitor of claim 19 wherein said glycidyl ether is defined by the formula:
wherein R 3 is an alkyl or substituted alkyl of 1-14 carbons or the atoms necessary to form at least one ethylene ether linkage.
21. The capacitor of claim 20 wherein said R 3 is an alkyl or substituted alkyl of 2-6 carbons.
22. The capacitor of claim 20 wherein said R 3 is a polyethylene ether.
23. The capacitor of claim 22 wherein said polyethylene ether has 2-220 polymerized ethylene ether groups.
24. The capacitor of claim 20 wherein said R 3 is an alkyl substituted with a group selected from the group consisting of hydroxy,
and
—(CH 2 OH) x CH 2 OH wherein X is 1 to 14.
25. The capacitor of claim 20 wherein said glycidyl ether is selected from the group consisting of:
where n is an integer of 1 to 220;
26. The capacitor of claim 1 further wherein said cathode further comprises a carboxylic acid.
27. The capacitor of claim 26 wherein said carboxylic acid is an aromatic acid with carboxylic groups.
28. The capacitor of claim 27 wherein said aromatic acid is selected from the group consisting of phthalic acid and benzoic acid.
29. The capacitor of claim 28 wherein said phthalic acid is ortho-phthalic acid.
30. The capacitor of claim 1 wherein said organic compound is a carboxylic crosslinking compound with two or more carboxylic acid groups.
31. The capacitor of claim 30 wherein said carboxylic crosslinking compound is aromatic acid with carboxylic groups.
32. The capacitor of claim 31 wherein said carboxylic crosslinking compound is selected from the group consisting of: oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, dodecanedioic acid, phthalic acids, maleic acid, muconic acid, citric acid, trimesic acid and polyacrylic acid.
33. A method for forming a capacitor comprising:
forming an anode;
forming a dielectric on said anode; and
forming a cathode on said dielectric comprising:
forming a conductive layer comprising:
applying an oxidant and 3,4-ethylenedioxythiophene) monomer to form poly(3,4-ethylenedioxythiophene) in-situ thereby forming a first conductive layer;
applying a conductive polymer dispersion over said first conductive layer wherein said conductive polymer dispersion comprises repeating units of —(CR 1 R 2 CR 3 R 4 ) wherein at least one of R 1 , R 2 , R 3 or R 4 comprises a group selected from thiophene, pyrrole or aniline with the proviso that none of R 1 , R 2 , R 3 or R 4 contain SOON or COOH;
0.0005 to 0.1000 grams of an organofunctional silane per gram of said conductive polymer dispersion; and
0.001 to 0.100 grams of an organic compound per gram of said conductive polymer dispersion with two or more functional groups selected from the group consisting of epoxy and carboxylic acid.
34. The method for forming a capacitor of claim 33 wherein said forming a cathode further comprises forming a carbon containing layer.
35. The method for forming a capacitor of claim 33 wherein said forming a cathode further comprises forming a metal containing layer.
36. The method for forming a capacitor of claim 33 wherein said applying a conductive polymer dispersion comprises applying a conductive polymer dispersion comprising said conductive polymer.
37. The method for forming a capacitor of claim 36 wherein said conductive polymer dispersion comprises at least one of said organofunctional silane or said organic compound.
38. The method for forming a capacitor of claim 37 wherein said conductive polymer dispersion comprises said organofunctional silane.
39. The method for forming a capacitor of claim 36 wherein said conductive polymer dispersion further comprises a polyanion.
40. The method for forming a capacitor of claim 39 wherein said polyanion is polystyrene sulfonic acid.
41. The method for forming a capacitor of claim 33 wherein said conductive polymer dispersion comprises a polythiophene.
42. The method for forming a capacitor of claim 41 wherein said polythiophene is poly(3,4-ethylenedioxy thiophene).
43. The method for forming a capacitor of claim 33 wherein said organofunctional silane is a glycidyl silane.
44. The method for forming a capacitor of claim 43 wherein said glycidyl silane is defined by the formula:
wherein R 1 is an alkyl of 1 to 14 carbons; and
each R 2 is independently an alkyl of 1 to 6 carbons.
45. The method for forming a capacitor of claim 44 wherein said R 1 is selected from the group consisting of methyl, ethyl and propyl.
46. The method for forming a capacitor of claim 44 wherein said glycidyl silane is:
47. The method for forming a capacitor of claim 33 wherein said organic compound is a glycidyl ether.
48. The method for forming a capacitor of claim 33 wherein said organofunctional silane is defined by the formula:
XR 1 Si(R 3 ) 3-n (R 2 ) n
wherein X is an organic functional group selected from the group consisting of amino, epoxy, anhydride, hydroxy, mercapto, sulfonate, carboxylate, phosphonate, halogen, vinyl, methacryloxy, ester and alkyl;
R 1 is an aryl or (CH 2 ) m wherein m can be 0 to 14;
R 2 is individually a hydrolysable functional group;
R 3 is individually an alkyl functional group of 1-6 carbons; and
n is 1 to 3.
49. The method for forming a capacitor of claim 48 wherein said hydrolysable functional group is selected from the group consisting of alkoxy, acyloxy, halogen and amine.
50. The method for forming a capacitor of claim 33 wherein said organofunctional silane is defined by the formula:
Y(Si(R 3 ) 3-n (R 2 ) n ) 2
wherein Y is any organic moiety that contains reactive or nonreactive functional groups, such as alkyl, aryl, sulfide or melamine;
R 2 is individually a hydrolysable functional group;
R 3 is individually an alkyl functional group of 1-6 carbons; and
n is 1 to 3.
51. The method for forming a capacitor of claim 33 wherein said organofunctional silane is selected from the group consisting of: 3-glycidoxypropyltrimethoxysilane, 3-aminopropytriethoxysilane, aminopropylsilanetriol, (triethoxysilyl)propylsuccinic anhydride, 3-mercaptoprpyltrimethoxysilane, vinyltrimethoxysilane, 3-metacryloxypropyltrimethoxysilane, 3-trihydroxysilyl-1-propane sulfonic acid and octyltriethyoxysilane.
52. The method for forming a capacitor of claim 33 wherein said organic compound is an epoxy crosslinking compound.
53. The method for forming a capacitor of claim 52 wherein said epoxy crosslinking compound is defined by the formula:
wherein the X is an alkyl or substituted alkyl of 0-14 carbons, an aryl or substituted aryl, an ethylene ether or substituted ethylene ether, polyethylene ether or substituted polyethylene ether with 2-20 ethylene ether groups or combinations thereof.
54. The method for forming a capacitor of claim 53 wherein said substitute is an epoxy group.
55. The method for forming a capacitor of claim 53 wherein alkyl or substituted alkyl has 0-6 carbons.
56. The method for forming a capacitor of claim 53 wherein said epoxy crosslinking is selected from the group consisting of: ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, 1,4-butanediol diglycidyl ether, pentylene glycol diglycidyl ether, hexylene glycol diglycidyl ether, cyclohexane dimethanol diglycidyl ether, resorcinol glycidyl ether, glycerol diglycidyl ether, glycerol polyglycidyl ethers, diglycerol polyglycidyl ethers, trimethylolpropane polyglycidyl ethers, sorbitol diglycidyl ether, sorbitol polyglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, polytetramethylene glycol diglycidyl ether, di(2,3-epoxypropyl) ether, 1,3-butadiene diepoxide, 1,5-hexadiene diepoxide, 1,2,7,8-diepoxyoctane, 1,2,5,6-Diepoxycyclooctane, 4-vinyl cyclohexene diepoxide, bisphenol diglycidyl ether and a maleimide-epoxy compound.
57. The method for forming a capacitor of claim 56 wherein said epoxy crosslinking compound is a glycidyl ether.
58. The method for forming a capacitor of claim 57 wherein said glycidyl ether is defined by the formula:
wherein R 3 is an alkyl or substituted alkyl of 1-14 carbons or the atoms necessary to form at least one ethylene ether linkage.
59. The method for forming a capacitor of claim 58 wherein said R 3 is an alkyl or substituted alkyl of 2-6 carbons.
60. The method for forming a capacitor of claim 58 wherein said R 3 is a polyethylene ether.
61. The method for forming a capacitor of claim 60 wherein said polyethylene ether has 2-220 polymerized ethylene ether groups.
62. The method for forming a capacitor of claim 58 wherein said R 3 is an alkyl substituted with a group selected from the group consisting of hydroxy,
and
—(CH 2 OH) x CH 2 OH wherein X is 1 to 14.
63. The method for forming a capacitor of claim 57 wherein said glycidyl ether is selected from the group consisting of:
where n is an integer of 1 to 220;
64. The method for forming a capacitor of claim 33 further wherein said cathode further comprises a carboxylic acid.
65. The method for forming a capacitor of claim 64 further wherein said carboxylic acid is an aromatic acid.
66. The method for forming a capacitor of claim 65 further wherein said aromatic acid is selected from the group consisting of phthalic acid and benzoic acid.
67. The method for forming a capacitor of claim 66 wherein said phthalic acid is ortho-phthalic acid.
68. The method for forming a capacitor of claim 33 wherein said organic compound is a carboxylic crosslinking compound with two or more carboxylic acid groups.
69. The method for forming a capacitor of claim 68 wherein said carboxylic crosslinking compound is aromatic acid with carboxylic groups.
70. The method for forming a capacitor of claim 69 wherein said carboxylic crosslinking compound is selected from the group consisting of: oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, dodecanedioic acid, phthalic acids, maleic acid, muconic acid, citric acid, trimesic acid and polyacrylic acid.
71. The capacitor of claim 1 wherein said anode comprises a pressed powder.
72. The capacitor of claim 1 further comprising decanediamine toluenesulfonate in alternating layers with said conductive polymer.
73. The method for forming a capacitor of claim 33 further comprising forming at least one decanediamine toluenesulfonate layer adjacent said conductive polymer dispersion layer.