IP Library Patent Application 11642697
Patent Application
App. No. 11/642,697

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.
11/642,697
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 (86)

1 . A process for forming a solar cell conductive feature, comprising:

(a) providing a precursor composition comprising first metallic nanoparticles, second metallic nanoparticles and liquid vehicle, wherein the first metallic nanoparticles comprise a first metal and the second metallic nanoparticles comprise a second metal or a metal oxide;

(b) depositing the precursor composition onto the substrate; and

(c) heating the precursor composition to form the solar cell conductive feature.

2 . The process of claim 1 , wherein the depositing comprises lithographic printing.

3 . The process of claim 1 , wherein the depositing comprises gravure printing.

4 . The process of claim 1 , wherein the depositing comprises flexo printing.

5 . The process of claim 1 , wherein the depositing comprises screen printing.

6 . The process of claim 1 , wherein the depositing comprises photopatterning.

7 . The process of claim 1 , wherein the depositing comprises drop on demand printing.

8 . The process of claim 1 , wherein the depositing comprises syringe printing.

9 . The process of claim 1 , wherein the depositing comprises aerosol jet depositing.

10 . The process of claim 1 , wherein the depositing comprises ink jet printing.

11 . The process of claim 10 , wherein the first metallic nanoparticles and the second metallic nanoparticles, collectively, have a bimodal particle size distribution.

12 . The process of claim 10 , wherein the first metallic nanoparticles and the second metallic nanoparticles are spherical.

13 . The process of claim 10 , wherein the first metallic nanoparticles have an average particle size of not greater than 100 nanometers.

14 . The process of claim 13 , wherein the second metallic nanoparticles have an average particle size of not greater than 100 nanometers.

15 . The process of claim 10 , wherein the first metallic nanoparticles have an average particle size of from about 10 to 80 nanometers.

16 . The process of claim 10 , wherein the first metallic nanoparticles have an average particle size of from about 25 to 75 nanometers.

17 . The process of claim 10 , wherein the second metallic nanoparticles have an average particle size of not greater than 100 nanometers.

18 . The process of claim 10 , wherein the second metallic nanoparticles have an average particle size of from about 10 to 80 nanometers.

19 . The process of claim 10 , wherein the second metallic nanoparticles have an average particle size of from about 25 to 75 nanometers.

20 . The process of claim 10 , wherein the second metallic nanoparticles comprise the second metal.

21 . The process of claim 20 , wherein the conductive feature comprises an alloy of the first metal and the second metal.

22 . The process of claim 10 , wherein the second metallic nanoparticles comprise the metal oxide.

23 . The process of claim 22 , wherein the metal oxide acts as an adhesion promoter.

24 . The process of claim 22 , wherein the metal oxide comprises silica, copper oxide, aluminum oxide or titania.

25 . The process of claim 22 , wherein the metal oxide comprises glass.

26 . The process of claim 22 , wherein the metal oxide comprises a conductive metal oxide.

27 . The process of claim 26 , wherein the conductive metal oxide comprises In 2 O 3 , indium-tin oxide, or antimony-tin oxide.

28 . The process of claim 22 , wherein the metal oxide comprises pyrogenous silica or surface modified silica.

29 . The process of claim 22 , wherein the metal oxide comprises aluminum borosilicate or lead borosilicate.

30 . The process of claim 22 , wherein the first metal is selected from the group consisting of silver, palladium, copper, gold, platinum and nickel.

31 . The process of claim 10 , wherein the heating comprises heating the precursor composition to a temperature not greater than 225° C. to form the solar cell conductive feature on the substrate.

32 . The process of claim 10 , wherein the heating comprises heating the precursor composition to a temperature not greater than 185° C. to form the solar cell conductive feature on the substrate.

33 . The process of claim 10 , wherein the substrate has a softening point of not greater than about 225° C.

34 . The process of claim 10 , wherein the substrate comprises a polymer.

35 . The process of claim 10 , wherein the substrate comprises a ceramic.

36 . The process of claim 10 , wherein the conductive feature comprises a set of finger lines and collector lines deposited essentially at a right angle to the finger lines.

37 . The process of claim 36 , wherein either or both the parallel finger lines or the collector lines have width of not less than 200 μm.

38 . The process of claim 36 , wherein either or both the parallel finger lines or the collector lines have width of not less than 100 μm.

39 . The process of claim 10 , wherein the conductive feature has a thickness greater than 1 μm.

40 . The process of claim 10 , wherein the conductive feature has a thickness greater than 5 μm.

41 . The process of claim 10 , wherein the conductive feature comprises a transparent conductive feature.

42 . The process of claim 10 , wherein the conductive feature comprises indium-tin oxide or antimony-tin oxide.

43 . The process of claim 10 , wherein the first metallic nanoparticles have a volume median particle size of not greater than 100 nm.

44 . The process of claim 43 , wherein the first metallic nanoparticles comprise a cap or coating thereon.

45 . The process of claim 44 , wherein the cap or coating comprises an inorganic cap or coating.

46 . The process of claim 44 , wherein the cap or coating comprises silica.

47 . The process of claim 44 , wherein the cap or coating comprises glass.

48 . The process of claim 44 , wherein the cap or coating comprises an organic cap or coating.

49 . The process of claim 44 , wherein the cap or coating comprises a polymer.

50 . The process of claim 44 , 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.

51 . The process of claim 44 , wherein the cap or coating comprises PVP.

52 . The process of claim 10 , wherein the conductive feature is resistant to solder leaching.

53 . The process of claim 10 , wherein the process further comprises high shear mixing the precursor composition.

54 . The process of claim 10 , wherein the process further comprises surface modifying the substrate with a laser.

55 . A precursor composition suitable for ink jet printing, the precursor composition comprising first metallic nanoparticles, second metallic nanoparticles and liquid vehicle, wherein the first metallic nanoparticles comprise a first metal and the second metallic nanoparticles comprise a second metal or a metal oxide.

56 . The precursor composition of claim 55 , wherein the precursor composition has a viscosity not greater than about 100 centipoise.

57 . The precursor composition of claim 55 , wherein the precursor composition has a viscosity not greater than about 50 centipoise.

58 . The precursor composition of claim 55 , wherein the first metallic nanoparticles and the second metallic nanoparticles, collectively, have a bimodal particle size distribution.

59 . The precursor composition of claim 55 , wherein the first metallic nanoparticles and the second metallic nanoparticles are spherical.

60 . The precursor composition of claim 55 , wherein the first metallic nanoparticles have an average particle size of not greater than 100 nanometers.

61 . The precursor composition of claim 60 , wherein the second metallic nanoparticles have an average particle size of not greater than 100 nanometers.

62 . The precursor composition of claim 55 , wherein the first metallic nanoparticles have an average particle size of from about 10 to 80 nanometers.

63 . The precursor composition of claim 55 , wherein the first metallic nanoparticles have an average particle size of from about 25 to 75 nanometers.

64 . The precursor composition of claim 55 , wherein the second metallic nanoparticles have an average particle size of not greater than 100 nanometers.

65 . The precursor composition of claim 55 , wherein the second metallic nanoparticles have an average particle size of from about 10 to 80 nanometers.

66 . The precursor composition of claim 55 , wherein the second metallic nanoparticles have an average particle size of from about 25 to 75 nanometers.

67 . The precursor composition of claim 55 , wherein the second metallic nanoparticles comprise the second metal.

68 . The precursor composition of claim 55 , wherein the second metallic nanoparticles comprise the metal oxide.

69 . The precursor composition of claim 68 , wherein the metal oxide comprises silica, copper oxide, aluminum oxide or titania.

70 . The precursor composition of claim 68 , wherein the metal oxide comprises glass.

71 . The precursor composition of claim 68 , wherein the metal oxide comprises a conductive metal oxide.

72 . The precursor composition of claim 71 , wherein the conductive metal oxide comprises In 2 O 3 , indium-tin oxide, or antimony-tin oxide.

73 . The precursor composition of claim 68 , wherein the metal oxide comprises pyrogenous silica or surface modified silica.

74 . The precursor composition of claim 68 , wherein the metal oxide comprises aluminum borosilicate or lead borosilicate.

75 . The precursor composition of claim 55 , wherein the first metal is selected from the group consisting of silver, palladium, copper, gold, platinum and nickel.

76 . The precursor composition of claim 55 , wherein the first metallic nanoparticles have a cap or coating thereon.

77 . The precursor composition of claim 76 , wherein the cap or coating comprises an inorganic cap or coating.

78 . The precursor composition of claim 76 , wherein the cap or coating comprises silica.

79 . The precursor composition of claim 76 , wherein the cap or coating comprises glass.

80 . The precursor composition of claim 76 , wherein the cap or coating comprises an organic cap or coating.

81 . The precursor composition of claim 76 , wherein the cap or coating comprises a polymer.

82 . The precursor composition of claim 76 , 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.

83 . The precursor composition of claim 76 , wherein the cap or coating comprises PVP.