IP Library Patent Application 11642699
Patent Application
App. No. 11/642,699

Low viscosity precursor compositions and methods for the deposition of conductive electronic features

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Quick Facts
Patent No.
US None
App. No.
11/642,699
Abstract

A precursor composition for the deposition and formation of an electrical feature such as a conductive feature. The precursor composition advantageously has a low viscosity enabling deposition using direct-write tools. The precursor composition also has a low conversion temperature, enabling the deposition and conversion to an electrical feature on low temperature substrates. A particularly preferred precursor composition includes silver metal for the formation of highly conductive silver features.

Claims (81)

1 . A process for forming a conductive feature on a flexible substrate, comprising:

(a) direct printing a precursor composition comprising metallic nanoparticles, a metal precursor compound to a metal and a liquid vehicle onto the flexible substrate; and

(b) heating the precursor composition to form the conductive feature on the flexible substrate.

2 . The process of claim 1 , wherein the direct printing comprises syringe printing.

3 . The process of claim 1 , wherein the direct printing comprises aerosol jet deposition.

4 . The process of claim 1 , wherein the direct printing comprises ink jet printing.

5 . The process of claim 4 , wherein the metallic nanoparticles comprise a metal selected from the group consisting of silver, palladium, copper, gold, platinum and nickel.

6 . The process of claim 4 , wherein the metallic nanoparticles have a volume median particle size of not greater than 100 nm.

7 . The process of claim 6 , wherein the metallic nanoparticles comprise a cap or coating thereon.

8 . The process of claim 7 , wherein the cap or coating comprises an organic cap or coating.

9 . The process of claim 7 , wherein the cap or coating comprises a polymer.

10 . The process of claim 7 , wherein the cap or coating comprises an intrinsically conductive polymer, a sulfonated perfluorohydrocarbon polymer, polystyrene, polystyrene/methacrylate, sodium bis(2-ethylhexyl) sulfosuccinate, tetra-n-octyl-ammonium bromide or an alkane thiolate.

11 . The process of claim 7 , wherein the cap or coating comprises PVP.

12 . The process of claim 6 , wherein at least 80 volume percent of the metallic nanoparticles are not larger than twice the average particle size.

13 . The process of claim 4 , wherein the metal is selected from the group consisting of silver, palladium, copper, gold, platinum and nickel.

14 . The process of claim 4 , wherein the conductivity of the conductive feature is no less than 10 percent the conductivity of the equivalent pure metal.

15 . The process of claim 4 , wherein the conductive feature has a resistivity that is not greater than 4 times the resistivity of the equivalent pure metal.

16 . The process of claim 4 , wherein the conductive feature has a resistivity that is not greater than 2 times the resistivity of the equivalent pure metal.

17 . The process of claim 4 , wherein the metallic nanoparticles comprise a second metal different from the metal formed from the metal precursor compound.

18 . The process of claim 4 , wherein the metallic nanoparticles comprise the same metal as the metal formed from the metal precursor compound.

19 . The process of claim 18 , wherein the conductivity of the conductive feature is no less than 10 percent the conductivity of the equivalent pure metal.

20 . The process of claim 18 , wherein the conductive feature has a resistivity that is not greater than 4 times the resistivity of the equivalent pure metal.

21 . The process of claim 18 , wherein the conductive feature has a resistivity that is not greater than 2 times the resistivity of the equivalent pure metal.

22 . The process of claim 4 , wherein the conductive feature has a width less than 200 μm.

23 . The process of claim 4 , wherein the conductive feature has a width less than 100 μm.

24 . The process of claim 4 , wherein the conductive feature has a thickness greater than 1 μm.

25 . The process of claim 4 , wherein the conductive feature has a thickness greater than 5 μm.

26 . The process of claim 4 , wherein the conductive feature comprises regions derived from the metallic nanoparticles dispersed in a matrix of the metal formed from the metal precursor compound.

27 . The process of claim 4 , wherein the heating sinters adjacent metallic nanoparticles to one another.

28 . The process of claim 4 , wherein the heating comprises heating the precursor composition to a temperature not greater than 300° C. to form the conductive feature on the substrate.

29 . The process of claim 4 , wherein the heating comprises heating the precursor composition to a temperature not greater than 225° C. to form the conductive feature on the substrate.

30 . The process of claim 4 , wherein the heating comprises heating the precursor composition to a temperature not greater than 185° C. to form the conductive feature on the substrate.

31 . The process of claim 4 , wherein the flexible substrate has a softening point of not greater than about 225° C.

32 . The process of claim 4 , wherein the flexible substrate has a softening point of not greater than about 185° C.

33 . The process of claim 4 , wherein the flexible substrate has a softening point of not greater than about 150C.

34 . The process of claim 4 , wherein the flexible substrate comprises a polyimide.

35 . The process of claim 4 , wherein the flexible substrate comprises.a polymer.

36 . The process of claim 4 , wherein the flexible substrate is selected from the group consisting of polyfluoronated compounds, polyimides, epoxies, polycarbonates, paper, acetate, polyester, polyethylene, polypropylene, polyvinyl chloride, acrylonitrile, butadiene, flexible fiber board, non-woven polymeric fabric, cloth, metallic foil and thin glass.

37 . The process of claim 4 , wherein the conductive feature comprises an electrode in a solar cell.

38 . The process of claim 4 , wherein the conductive feature is employed in a flat panel display.

39 . The process of claim 4 , wherein the conductive feature comprises a transparent conductive feature.

40 . The process of claim 4 , wherein the conductive feature comprises indium-tin oxide or antimony-tin oxide.

41 . The process of claim 4 , wherein the process further comprises surface modifying the substrate with a laser.

42 . The process of claim 41 , wherein the laser increases or decreases the hydrophilicity of the substrate.

43 . A process for forming a conductive feature on a flexible substrate, the process comprising heating an ink jet printed precursor composition to form the conductive feature on the flexible substrate, wherein the precursor composition comprises metallic nanoparticles, a metal precursor compound to a metal and a liquid vehicle.

44 . The process of claim 43 , wherein the metallic nanoparticles comprise a metal selected from the group consisting of silver, palladium, copper, gold, platinum and nickel.

45 . The process of claim 43 , wherein the metallic nanoparticles have a volume median particle size of not greater than 100 nm.

46 . The process of claim 45 , wherein the metallic nanoparticles comprise a cap or coating thereon.

47 . The process of claim 46 , wherein the cap or coating comprises an organic cap or coating.

48 . The process of claim 47 , wherein the cap or coating comprises a polymer.

49 . The process of claim 47 , wherein the cap or coating comprises an intrinsically conductive polymer, a sulfonated perfluorohydrocarbon polymer, polystyrene, polystyrene/methacrylate, sodium bis(2-ethylhexyl) sulfosuccinate, tetra-n-octyl-ammonium bromide or an alkane thiolate.

50 . The process of claim 47 , wherein the cap or coating comprises PVP.

51 . The process of claim 46 , wherein at least 80 volume percent of the metallic nanoparticles are not larger than twice the average particle size.

52 . The process of claim 43 , wherein the metal is selected from the group consisting of silver, palladium, copper, gold, platinum and nickel.

53 . The process of claim 43 , wherein the conductivity of the conductive feature is no less than 10 percent the conductivity of the equivalent pure metal.

54 . The process of claim 43 , wherein the conductive feature has a resistivity that is not greater than 4 times the resistivity of the equivalent pure metal.

55 . The process of claim 43 , wherein the conductive feature has a resistivity that is not greater than 2 times the resistivity of the equivalent pure metal.

56 . The process of claim 43 , wherein the metallic nanoparticles comprise a second metal different from the metal formed from the metal precursor compound.

57 . The process of claim 43 , wherein the metallic nanoparticles comprise the same metal as the metal formed from the metal precursor compound.

58 . The process of claim 57 , wherein the conductivity ofthe conductive feature is no less than 10 percent the conductivity of the equivalent pure metal.

59 . The process of claim 57 , wherein the conductive feature has a resistivity that is not greater than 4 times the resistivity of the equivalent pure metal.

60 . The process of claim 57 , wherein the conductive feature has a resistivity that is not greater than 2 times the resistivity of the equivalent pure metal.

61 . The process of claim 43 , wherein the conductive feature has a width less than 200 μm.

62 . The process of claim 43 , wherein the conductive feature has a width less than 100 μm.

63 . The process of claim 43 , wherein the conductive feature has a thickness greater than 1 μm.

64 . The process of claim 43 , wherein the conductive feature has a thickness greater than 5 μm.

65 . The process of claim 43 , wherein the conductive feature comprises regions derived from the metallic nanoparticles dispersed in a matrix of the metal formed from the metal precursor compound.

66 . The process of claim 43 , wherein the heating sinters adjacent metallic nanoparticles to one another.

67 . The process of claim 43 , wherein the heating comprises heating the precursor composition to a temperature not greater than 300° C. to form the conductive feature on the substrate.

68 . The process of claim 43 , wherein the heating comprises heating the precursor composition to a temperature not greater than 225° C. to form the conductive feature on the substrate.

69 . The process of claim 43 , wherein the heating comprises heating the precursor composition to a temperature not greater than 185° C. to form the conductive feature on the substrate.

70 . The process of claim 43 , wherein the flexible substrate has a softening point of not greater than about 225° C.

71 . The process of claim 43 , wherein the flexible substrate has a softening point of not greater than about 185° C.

72 . The process of claim 43 , wherein the flexible substrate has a softening point of not greater than about 150° C.

73 . The process of claim 43 , wherein the flexible substrate comprises a polyimide.

74 . The process of claim 43 , wherein the flexible substrate comprises a polymer.

75 . The process of claim 43 , wherein the flexible substrate is selected from the group consisting of polyfluoronated compounds, polyimides, epoxies, polycarbonates, paper, acetate, polyester, polyethylene, polypropylene, polyvinyl chloride, acrylonitrile, butadiene, flexible fiber board, non-woven polymeric fabric, cloth, metallic foil and thin glass.

76 . The process of claim 43 , wherein the conductive feature comprises an electrode in a solar cell.

77 . The process of claim 43 , wherein the conductive feature is employed in a flat panel display.

78 . The process of claim 43 , wherein the conductive feature comprises a transparent conductive feature.

79 . The process of claim 43 , wherein the conductive feature comprises indium-tin oxide or antimony-tin oxide.