Buffer layer for sintering

Information

  • Patent Grant
  • 9131610
  • Patent Number
    9,131,610
  • Date Filed
    Thursday, November 7, 2013
    11 years ago
  • Date Issued
    Tuesday, September 8, 2015
    9 years ago
Abstract
A layer of material having a low thermal conductivity is coated over a substrate. A film of conductive ink is then coated over the layer of material having the low thermal conductivity, and then sintered. The film of conductive ink does not absorb as much energy from the sintering as the film of conductive ink coated over the layer of material having the low thermal conductivity. The layer of material having the low thermal conductivity may be a polymer, such as polyimide.
Description
BACKGROUND INFORMATION

The microelectronics and semiconductor packaging industries have begun to shift to printable electronics. Electronics circuits comprise a variety of components that are electrically connected to each other. Such electrical connections between different components may be made of conductive metal traces that can be printed on substrates with conductive inks. The inks are processed and sintered after deposition on a substrate in order to become conductive. Thermal sintering uses a high temperature (e.g., ≧250° C. to fuse the nanoparticles in the inks. Photonic (photo) and laser sintering utilize a very high intensity lamp/laser to fuse the nanoparticles in a very short period of time (e.g., microseconds) with a low temperature and so as not to damage the underlying substrates. However, the photo/laser sintering process has limits that require low thermal conductivity material for substrates in order for the nanoparticles to effectively absorb energy and sinter before heat energy dissipates into the substrate. In other words, the substrates that can be used in these applications will be very limited for low thermal conductivity materials.


On the other hand, low thermal conductive substrates can be used for flexible printable electronics. Low temperature melting point materials such as polyethylene (PE), polyester (PET), etc., will prevent the nanoparticle inks from proper sintering, and the substrates will be damaged, with the result that the resistivity will be very high.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a digital photograph showing copper inks photosintered on four silicon wafers.



FIG. 2 is a digital photograph showing copper inks before being photosintered.



FIG. 3 is a digital photograph showing copper inks after being photosintered.



FIG. 4 is a digital photograph showing laser sintered lines on a Kapton substrate.



FIG. 5 is an enlarged digital photograph showing the laser sintered lines of FIG. 4.



FIG. 6 illustrates a graph showing that copper ink resistivity sintered by a laser is not only inversely proportional to laser power, but also inversely proportional to buffer layer thickness made of polyimide.



FIG. 7 illustrates a graph showing thicknesses of cured polyimide measured at various spin speeds.



FIG. 8 illustrates a graph showing that resistivity of sintered copper film is inversely proportional to polyimide thickness.



FIG. 9 illustrates a graph showing that adhesion of copper ink film to polyimide is proportional to polyimide thickness.



FIG. 10 illustrates a graph showing that laser writing line width is proportional to the laser power density.



FIGS. 11A-11F illustrate a process in accordance with embodiments of the present invention.





DETAILED DESCRIPTION

Embodiments of the present invention disclose a photosintering process to effectively sinter metallic nanoparticles on a polyimide substrate, thus causing the film to be very conductive near the bulk material. On other hand, the photosintering process does not perform well on nanoparticle inks coated on substrates possessing a high thermal conductivity, such as ceramics and silicon wafer. Table 1 shows the thermal conductivity for a variety of materials.















TABLE 1









heat

melting




density
heat capacity
conductivity
thermal
point, ° C.


item #
material
(g/cm3)
(J/g · K)
(W/m · K)
effusivity
degrees





















1
air
0.0013
1
0.025
0.00
NA


2
paper
0.33
0.73
0.030
0.01
NA


3
Polyimide (kapton)
1.42
1.09
0.120
0.19
NA


4
PMMA (resist)
1.19
1.46
0.160
0.28
180


5
PET (Mylar)
1.23
1.13
0.176
0.24
150


6
LCP (liquid crystal
1.4
1.6
0.500
1.12
300



polymer)


7
PE (polyethylene,
0.95
2.3
0.500
1.09
125



high density)


8
water
1
4.2
0.600
2.52
0


9
glass
2.3
0.753
1.330
2.30
950


10
SiO2
2.2
0.75
1.380
2.28
1600


11
MgO
3.2
0.84
5.900
15.86
2852


12
carbon-amorphous
1.51
0.707
6.280
6.70
3600


13
Si3N4
2.8
0.69
7.950
15.36
1900


14
TiO2
4.25
0.69
9.000
26.39
1843


15
CuO/Cu2O
6.5
0.536
18.000
62.71
1235


16
Ti
4.5
0.523
21.000
49.42
1668


17
Al2O3 (ceramics)
2.5
0.81
30.000
60.75
2054


18
solder (60/40
8.5
0.197
50.210
84.08
185



Sn/Pb)


19
Ni
8.9
0.444
88.000
347.74
1455


20
Mo
10.2
0.25
134.000
341.70
2623


21
Si
2.33
0.7
148.000
241.39
1414


22
carbon-graphite
2.25
0.707
167.360
266.23
3600


23
Al
2.7
0.88
209.000
496.58
660


24
Au
19.3
0.13
318.000
797.86
1086


25
Cu
8.9
0.385
398.000
1363.75
1064


26
carbAL
2.3
0.75
425.000
733.13
3600


27
Ag
10.5
0.24
427.000
1076.04
962


28
carbon-diamond
3.51
0.506
543.920
966.03
3800


29
carbon nanotubes


6000.000









Low conductivity materials, such as polyimide, can be used as a coating material onto other high thermal conductivity substrates, such as ceramics and silicon wafer, in order to isolate heat energy dissipation from nanoparticles during a photosintering process so that the nanoparticles are fused more effectively. How quickly heat dissipates depends on the thickness of the low thermal conductivity material (e.g., polyimide film).


The following experiment was conducted for showing how the present invention operates. Three wafers were spin coated with 1, 1.5, and 2.3 microns thick DuPont PI-2610 polyimide, respectively, and thermal cured at 350° C. for 30 minutes. One bare silicon wafer was used for a reference (wafer #1). All four wafers were coated with copper ink using a drawdown process. After a 60 minute drying process at 100° C., each wafer was divided into three zones that were individually sintered with three different energy levels. The resistance for each zone and each wafer was measured with a voltmeter, with the results shown in Table 2, which shows the electrical resistances of a copper film after photosintering with various coating thicknesses of polyimide on silicon wafers.














TABLE 2








Zone 1:
Zone 2:
Zone 3:



polyimide
copper
resistance
resistance
resistance with


wafer #
thickness (μm)
ink (μm)
with energy 1
with energy 2
energy 3





















1
0
3.2
>20 MΩ
>20 MΩ
>20



2
1
3.2
>20 MΩ
>20 MΩ
>20



3
1.5
3.2
>20 MΩ
>20 MΩ
>20



4
2.3
3.2
>20 MΩ
>20 MΩ
20
Ω





where


energy 1 = 3 sinter shots with 850/1050 V, 1000 μsec


energy 2 = 4 sinter shots with 850/1150 V, 1000 μsec


energy 3 = 5 sinter shots with 850/1250 V, 2000 μsec






Except for zone 3 of wafer 4, all zones from the four wafers did not experience a change in resistance after photosintering. Zone 3 of wafer 4 experienced a change in its metallic color at the highest energy level, as shown in FIG. 1. The area had a severe blow off. The surrounding area had copper debris left that was conductive. This is clear evidence that the polyimide material may be used as a thermal insulator. The thickness of polyimide may be more than 3 microns. The thermal conductivity is 0.12 and 148 W/m·K for polyimide and silicon, respectively. The heat dissipated into the silicon substrate (wafer #1) too quickly to sinter the copper nanoparticles since there was no polyimide material.


Wafers 1, 2, and 3 all had high resistance (greater than 20 mega-ohms). Wafer 4 at the center zone with 20 ohms resistance as shown in FIG. 1 appeared that the copper nanoparticies film started to be fused, sintered, and turned into a copper color. The thicker low thermal conductivity material can thus be used as a good thermal insulator.


In addition to the liquid polyimide disclosed above, a dry polyimide film was also utilized. The copper ink was coated on a 50 micron polyimide film (e.g., Kapton). The sample was placed on a silicon wafer and a carbAL high thermal conductive heat sink, as shown in FIG. 2. Silicon grease was coated in between the polyimide film and the silicon wafer and heat sink to ensure good thermal contact. The sample was photosintered simultaneously in a single shot. The copper was sintered very well and turned a shiny copper color, as shown in FIG. 3. It did not matter what materials the polyimide film was residing on. At least a 50 micron thick polyimide film is sufficiently thick to isolate and prevent heat energy dissipation for photosintering processes, though a thickness of less than 50 microns may be utilized for embodiments where less conductivity is desired of the conductive traces.


In addition, laser sintering was utilized on silicon wafers with the same setup as described above. The laser was a solid state diode with an 830 nm wavelength and an 800 mW power. The focus beam size was 15 microns in diameter and controlled by a collimator and an objective lens, as shown in FIGS. 4 and 5.


This laser had sufficient power to sinter and fuse the nanoparticies and turn the copper ink conductive. There were four silicon wafers coated with various polyimide thicknesses of 1, 1.5, 2, and 3 microns, respectively, along with a bare silicon wafer as a reference. The resistivity of each wafer is plotted with laser power in FIG. 6, which indicates that the copper film conductivity is proportional to the polyimide thickness, and the heat generated by the laser is transferred to the substrate less with polyimide present than the bare silicon wafer without polyimide. This is clear evidence that any material having a low thermal conductivity, such as a polyimide material, may be used as a thermal insulator and enhance the photograph and laser sintering processes.


Furthermore, a variety of polyimide thicknesses were coated on silicon wafers and cured at 350° C. for one hour. Then the standard copper ink was coated by drawdown, dried in an oven, and photo/laser sintered. Electrical measurements were performed and characterized the copper ink samples.


Three types of polyimide material (e.g. made by DuPont) were used to spin coat on silicon wafer at 1000, 2000, 3000, 4000, and 5000 rpm. FIG. 7 illustrates a graph showing thicknesses of cured polyimide measured at various spin speeds. The range was from 1 to 20 microns on each wafer, respectively.


After samples were prepared, both photograph and laser sintering were performed on the copper inks. Different types of sintering were compared versus resistivity and adhesion, as well as line width for laser sintering. Table 3 shows samples photosintered at the same energy level with various thicknesses of polyimide. Table 4 shows samples laser sintered at a fixed power level with various thicknesses of polyimide,













TABLE 3





sample
polyimide
Cu ink thickness
resistivity
adhesion


#
thickness (μm)
(μm)
(ohm-cm)
(1-10)



















1
0
3
3.00 × 101
1


2
5
2
1.30 × 10−4
2


3
6.5
2
4.00 × 10−5
4


4
8.7
2
1.60 × 10−5
7


5
12.5
2
1.52 × 10−5
7


6
10
1.5
1.50 × 10−5
8


7
14
1.5
1.40 × 10−5
8


8
20
1.5
1.14 × 10−5
8





















TABLE 4






polyimide
resistivity

line width
line width



thickness
(ohm-cm) at
adhesion
(μm) at
(μm) at


sample #
(μm)
840 mW
(1-10)
840 mW
409 mW




















11
0
1.60 × 10−4
1
70
35


12
1
1.26 × 10−5
5
74
38


13
1.5
1.36 × 10−5
5
77
39


14
2
9.33 × 10−6
3
83
40


15
3
6.00 × 10−6
1
88
42


16
5
4.75 × 10−6
8
92
65


17
7
4.82 × 10−6
8
103
75


18
12
3.61 × 10−6
8
150
88


19
20
5.47 × 10−6
8
180
120










FIG. 8 illustrates a graph showing that resistivity of sintered copper film is inversely proportional to polyimide thickness. The saturated points for resistivity are approximately at 10 microns for photosintering and approximately at 5 microns for laser sintering. Power density of photosintering is much lower than that of laser sintering, providing a reason why its resistivity is higher.



FIG. 9 illustrates a graph showing that adhesion of copper ink film to polyimide is proportional to polyimide thickness. There are some noise points, but the trend is clear from the graph. The thicker the polyimide is, the better the adhesion is. Again, critical points of polyimide thickness for the good adhesion are approximately at 10 microns for photosintering and approximately at 5 microns for laser sintering.



FIG. 10 illustrates a graph showing that laser writing line width is proportional to the laser power density. With given laser power, the laser writing line width is also proportional to the polyimide film thickness, providing more evidence that polyimide is a good thermal, insulator for these processes. The laser energy and heat deposited on the copper ink surface could not spread any deeper vertically but laterally while the polyimide thickness increased.


Referring to FIGS. 11A-11F, a process for performing embodiments of the present invention is illustrated. A substrate 1101 is provided on which electronic circuitry is to be mounted. In FIG. 11B, traces of a metal material 1102 are deposited in a desired pattern on the substrate 1101, using a well-known manufacturing process. In FIG. 11C, a layer of low thermal conductivity material 1103, such as polyimide, is coated over the metal traces 1102 and substrate 1101. To create further patterns for the conductive traces to be deposited, vias 1104 are formed through the material 1103, exposing portions of the metal traces 1102. In FIG. 11E, an ink jet apparatus 1106 deposits a conductive ink 1105, such as copper nanoparticles, over the material 1103 and the metal traces 1102 exposed by the vias 1104. In FIG. 11F a photograph or laser sintering process is performed on the deposited conductive ink nanoparticles 1105 to sinter them into conductive traces 1107, as described herein. Depositing of the conductive inks and the sintering processes are described in U.S. Patent Publication No. 2008/0286488 A1, which is hereby incorporated by reference herein.


SUMMARY

1. The effectiveness of a photosintering process depends on not only metallic nanoparticle size, but also the type of substances.


2. Effective photosintering is achieved with nanoparticles below 300 nm.


3. The thermal conductivity of substrates will affect metallic ink photosintering. The lower the thermal conductivity of the substrate, the better the electrical conductivity of the nanoparticle film.


4. High thermal conductive substrates can be tailored and isolated by coating low thermal conductivity material, such as polyimide or polymer, for an effective photosintering process.


5. The thickness of coating of polyimide required to isolate thermal heat dissipation is approximately 1-50 microns.


6. The copper ink becoming a conductive film has been demonstrated on high thermal conductive material such as silicon wafer with both laser and photosintering.


7. Heat dissipation on high thermal conductive silicon wafers has been shown with a variety of polyimide thicknesses coated on a wafer. A low thermal conductive material can be used as a buffer layer to slow down heat dissipation and enhance the photograph or laser sintering.


8. Copper ink may be sintered well with polyimide coated on a silicon wafer with resistivity at 1×10−5 ohm-cm by photosintering and 4×10−6 ohm-cm by laser sintering.


9. The polyimide material may be not only utilized as a heat insulator on high thermal conductive substrates and enhance copper ink photograph and laser sintering effectiveness, but also applied to low melting temperature substrates as a heat insulator to protect from heat damage during a sintering process.


10. Polyimide layer and metal trace layer can be repeated several times as multilayer circuits.


11. Polyimide layer can be used as a dielectric material and incorporated as capacitors.


12. Nano-copper ink can be used at top layer conductor as a contact metal in two-dimensional and three-dimensional chip packaging applications.

Claims
  • 1. A method comprising: coating a layer of material having a low thermal conductivity over a substrate;depositing a film of conductive ink over the layer of material having the low thermal conductivity; andsintering the film of conductive ink.
  • 2. The method as recited in claim 1, further comprising: depositing a metal layer in a pattern on the substrate, wherein the layer of material having the low thermal conductivity is coated over the patterned metal layer and the substrate; andforming a via through the layer of material having the low thermal conductivity thereby exposing a portion of the patterned metal layer, wherein the depositing of the film of conductive ink includes depositing the film of conductive ink into the via to thereby coat the portion of the patterned metal layer with the film of conductive ink, wherein the film of conductive ink coating the portion of the patterned metal layer is also sintered.
  • 3. The method as recited in claim 1, wherein the substrate has a thermal conductivity greater than the layer of material having the low thermal conductivity.
  • 4. The method as recited in claim 2, wherein the film of conductive ink coated over the portion of the patterned metal layer does not dissipate as much energy from the sintering as the film of conductive ink coated over the layer of material having the low thermal conductivity.
  • 5. The method as recited in claim 4, wherein the layer of material having the low thermal conductivity comprises a polymer.
  • 6. The method as recited in claim 4, wherein the layer of material having the low thermal conductivity comprises polyimide.
  • 7. The method as recited in claim 6, wherein the polyimide has a thickness of at least 50 microns.
  • 8. The method as recited in claim 6, wherein the sintering is performed with a photosintering apparatus.
  • 9. The method as recited in claim 6, wherein the sintering is performed with a laser sintering apparatus.
  • 10. The method as recited in claim 6, wherein the substrate comprises silicon.
  • 11. The method as recited in claim 6, wherein the substrate comprises a ceramic.
  • 12. The method as recited in claim 6, wherein the film of conductive ink comprises copper nanoparticles.
  • 13. The method as recited in claim 6, wherein the polyimide has a thickness of at least 5 microns.
  • 14. The method as recited in claim 6, wherein the polyimide has a thickness of at least 2.3 microns.
  • 15. The method as recited in claim 9, wherein the laser sintering apparatus comprises a solid state diode with an 830 nm wavelength and 800 mW power.
  • 16. The method as recited in claim 15, wherein the solid state diode has a focus beam size of 15 microns in diameter.
  • 17. A method comprising: coating a layer of material having a low thermal conductivity as a buffer layer over a substrate;depositing a film of conductive ink over the layer of material having the low thermal conductivity; andphotonic or laser sintering the film of conductive ink with a photo or laser sintering apparatus.
  • 18. The method as recited in claim 17, further comprising: depositing a metal layer in a pattern on the substrate, wherein the layer of material having the low thermal conductivity is coated over the patterned metal layer and the substrate; andforming a via through the layer of material having the low thermal conductivity thereby exposing a portion of the patterned metal layer, wherein the depositing of the film of conductive ink includes depositing the film of conductive ink into the via to thereby coat the portion of the patterned metal layer with the film of conductive ink, wherein the film of conductive ink coating the portion of the patterned metal layer is also sintered.
  • 19. The method as recited in claim 17, wherein the layer of material having the low thermal conductivity comprises a polymer or polyimide, wherein the substrate has a thermal conductivity greater than the layer of material having the low thermal conductivity.
  • 20. The method as recited in claim 18, wherein the film of conductive ink coated over the portion of the patterned metal layer does not dissipate as much energy from the sintering as the film of conductive ink coated over the layer of material having the low thermal conductivity.
Parent Case Info

This application is a continuation of U.S. patent application Ser. No. 13/260,893, which claims priority to U.S. Provisional Patent Application Ser. Nos. 61/174,758 and 61/163,894.

US Referenced Citations (211)
Number Name Date Kind
3239597 Flynn Mar 1966 A
3580731 Milewski et al. May 1971 A
3796598 Gejyo et al. Mar 1974 A
3950605 Hori et al. Apr 1976 A
4093466 Davis Jun 1978 A
4151008 Kirkpatrick Apr 1979 A
4194913 Davis Mar 1980 A
RE30434 Davis Nov 1980 E
4234631 Davis Nov 1980 A
4331518 Wilson May 1982 A
4591951 Iwamoto et al. May 1986 A
4640746 Nobel et al. Feb 1987 A
4681670 Nobel et al. Jul 1987 A
4749626 Kadija et al. Jun 1988 A
4756791 D'Angelo et al. Jul 1988 A
4922322 Mathew May 1990 A
4935312 Nakayama et al. Jun 1990 A
4959278 Shimauch et al. Sep 1990 A
4997516 Adler Mar 1991 A
4997722 Adler Mar 1991 A
5008997 Phy Apr 1991 A
5039576 Wilson Aug 1991 A
5049718 Spletter et al. Sep 1991 A
5130275 Dion Jul 1992 A
5160422 Nishimura et al. Nov 1992 A
5202179 Kasahara Apr 1993 A
5234513 Inoue et al. Aug 1993 A
5260849 Kasahara Nov 1993 A
5277756 Dion Jan 1994 A
5320737 Chao et al. Jun 1994 A
5322823 Ueda et al. Jun 1994 A
5384204 Yumoto et al. Jan 1995 A
5393573 MacKay Feb 1995 A
5439639 Vianco et al. Aug 1995 A
5492595 Carano et al. Feb 1996 A
5698087 Bokisa Dec 1997 A
5724727 Chopra et al. Mar 1998 A
5730851 Arrowsmith et al. Mar 1998 A
5750017 Zhang May 1998 A
5798286 Faraci et al. Aug 1998 A
5807519 Suzuki et al. Sep 1998 A
5861076 Adlam Jan 1999 A
5879568 Urasaki et al. Mar 1999 A
5889083 Zhu et al. Mar 1999 A
5990197 Escano et al. Nov 1999 A
6010771 Isen et al. Jan 2000 A
6093503 Isoyama et al. Jul 2000 A
6099713 Yanada et al. Aug 2000 A
6139777 Omoya et al. Oct 2000 A
6147400 Faraci et al. Nov 2000 A
6165386 Endo et al. Dec 2000 A
6200732 Tamura et al. Mar 2001 B1
6238847 Axtell et al. May 2001 B1
6248455 Adams et al. Jun 2001 B1
6297142 Mita et al. Oct 2001 B1
6306947 Morishima et al. Oct 2001 B1
6361823 Bokisa et al. Mar 2002 B1
6426548 Mita et al. Jul 2002 B1
6433409 Mita et al. Aug 2002 B2
6472459 Morales et al. Oct 2002 B2
6530944 West et al. Mar 2003 B2
6554914 Rozbicki et al. Apr 2003 B1
6583500 Abbott et al. Jun 2003 B1
6603205 Miura Aug 2003 B2
6638847 Cheung et al. Oct 2003 B1
6646330 Kubara et al. Nov 2003 B2
6651521 Carbone et al. Nov 2003 B2
6664492 Babb et al. Dec 2003 B1
6679937 Kodas et al. Jan 2004 B1
6682584 Pozarnsky et al. Jan 2004 B2
6720499 Bokisa et al. Apr 2004 B2
6773827 Higuchi Aug 2004 B2
6773828 Ooi et al. Aug 2004 B1
6774036 Goldstein Aug 2004 B2
6783569 Cheon et al. Aug 2004 B2
6828660 Abbott Dec 2004 B2
6860981 Schetty, III et al. Mar 2005 B2
6899775 Hill et al. May 2005 B2
6917098 Yamunan Jul 2005 B1
6951666 Kodas et al. Oct 2005 B2
7019391 Tran Mar 2006 B2
7062848 Pan et al. Jun 2006 B2
7084067 Geusic et al. Aug 2006 B2
7087523 Grigoropoulos et al. Aug 2006 B2
7153775 Geusic Dec 2006 B2
7160629 Crosby Jan 2007 B2
7179362 Dietterle et al. Feb 2007 B2
7195702 Bokisa, Sr. et al. Mar 2007 B2
7215014 Su et al. May 2007 B2
7252699 Perry et al. Aug 2007 B2
7262603 Benton et al. Aug 2007 B1
7294366 Renn et al. Nov 2007 B2
7297902 Weiss Nov 2007 B2
7316725 Kodas et al. Jan 2008 B2
7351667 Hwang et al. Apr 2008 B2
7357681 Yamagami et al. Apr 2008 B2
7384862 Yamazaki Jun 2008 B2
7391116 Chen et al. Jun 2008 B2
7482540 Shukushima et al. Jan 2009 B2
7507618 Dunbar Mar 2009 B2
7514369 Li et al. Apr 2009 B2
7547479 Wessling Jun 2009 B2
7776196 Fujimoto et al. Aug 2010 B2
7786024 Stumbo et al. Aug 2010 B2
7867413 Lee et al. Jan 2011 B2
7879131 Yaniv et al. Feb 2011 B2
8647979 Yaniv et al. Feb 2014 B2
20020148386 Woosman et al. Oct 2002 A1
20020158342 Tuominen et al. Oct 2002 A1
20020185716 Abys et al. Dec 2002 A1
20020187364 Heber et al. Dec 2002 A1
20020192492 Abys Dec 2002 A1
20030025182 Abys et al. Feb 2003 A1
20030151030 Gurin Aug 2003 A1
20030168639 Cheon et al. Sep 2003 A1
20030213614 Furusawa Nov 2003 A1
20030226758 Egli Dec 2003 A1
20040026256 Lindgren Feb 2004 A1
20040026684 Empedocies Feb 2004 A1
20040118696 Zhang et al. Jun 2004 A1
20040131934 Sugnaux et al. Jul 2004 A1
20040132299 Matsuda et al. Jul 2004 A1
20040134379 Wong et al. Jul 2004 A1
20040147113 Yamazaki et al. Jul 2004 A1
20040147618 Lee et al. Jul 2004 A1
20040171211 Lee et al. Sep 2004 A1
20040175631 Crocker et al. Sep 2004 A1
20040192042 Sirringhaus et al. Sep 2004 A1
20040218136 Imai et al. Nov 2004 A1
20040232000 Crosby Nov 2004 A1
20040241532 Kim Dec 2004 A1
20040256239 Whitlaw et al. Dec 2004 A1
20050019543 Lyles Jan 2005 A1
20050026423 Yamazaki Feb 2005 A1
20050078158 Magdassi et al. Apr 2005 A1
20050097987 Kodas et al. May 2005 A1
20050145502 Schetty, III et al. Jul 2005 A1
20050148164 Casey et al. Jul 2005 A1
20050183768 Roscheisen et al. Aug 2005 A1
20050218398 Tran Oct 2005 A1
20050230042 Hasimoto Oct 2005 A1
20050249967 Egli Nov 2005 A1
20050249968 Xu et al. Nov 2005 A1
20050249969 Xu et al. Nov 2005 A1
20050274480 Barsoum et al. Dec 2005 A1
20060001726 Kodas et al. Jan 2006 A1
20060011267 Kay et al. Jan 2006 A1
20060054668 Severin Mar 2006 A1
20060057502 Okada et al. Mar 2006 A1
20060062701 Nakamura et al. Mar 2006 A1
20060068218 Hooghan Mar 2006 A1
20060073680 Han et al. Apr 2006 A1
20060082952 Ogiwara Apr 2006 A1
20060090819 Egli May 2006 A1
20060091121 Zanolli et al. May 2006 A1
20060096867 Bokisa et al. May 2006 A1
20060110424 Lyles May 2006 A1
20060111467 Reinhardt et al. May 2006 A1
20060116000 Yamamoto Jun 2006 A1
20060141268 Kalkan et al. Jun 2006 A1
20060159838 Kowalski et al. Jul 2006 A1
20060163743 Kuwabara et al. Jul 2006 A1
20060163744 Vanheusden et al. Jul 2006 A1
20060183055 O'Neill et al. Aug 2006 A1
20060189113 Vanheusden et al. Aug 2006 A1
20060234519 Pan et al. Oct 2006 A1
20060240591 Grier et al. Oct 2006 A1
20060286301 Murata et al. Dec 2006 A1
20070007144 Schetty, III Jan 2007 A1
20070040191 Bezryadin et al. Feb 2007 A1
20070051927 Itoh et al. Mar 2007 A1
20070074316 Alden et al. Mar 2007 A1
20070095879 Holmes May 2007 A1
20070105395 Kinzel et al. May 2007 A1
20070117475 Tu May 2007 A1
20070144305 Jablonski et al. Jun 2007 A1
20070145375 Cho Jun 2007 A1
20070148972 Hara et al. Jun 2007 A1
20070158204 Taylor et al. Jul 2007 A1
20070163643 Van Duren Jul 2007 A1
20070166453 Van Duren et al. Jul 2007 A1
20070175296 Subramanian et al. Aug 2007 A1
20070176991 Arai et al. Aug 2007 A1
20070190326 Perry et al. Aug 2007 A1
20070218312 Sakuyama et al. Sep 2007 A1
20070275262 Lin et al. Nov 2007 A1
20070281136 Hampden-Smith et al. Dec 2007 A1
20070281249 Tutt et al. Dec 2007 A1
20070284700 Jackson et al. Dec 2007 A1
20070287022 Jackson et al. Dec 2007 A1
20070287023 Jackson et al. Dec 2007 A1
20070287024 Jackson et al. Dec 2007 A1
20070289483 Cho et al. Dec 2007 A1
20070295530 Jackson et al. Dec 2007 A1
20080020208 Lee et al. Jan 2008 A1
20080020304 Schroder et al. Jan 2008 A1
20080075934 Barlow et al. Mar 2008 A1
20080083950 Pan et al. Apr 2008 A1
20080143906 Allemand et al. Jun 2008 A1
20080164557 Kim et al. Jul 2008 A1
20080169122 Shiraishi et al. Jul 2008 A1
20080193667 Garbar et al. Aug 2008 A1
20080241391 Kim et al. Oct 2008 A1
20080241414 Kim et al. Oct 2008 A1
20080286488 Li et al. Nov 2008 A1
20080305268 Norman et al. Dec 2008 A1
20090142481 Chopra et al. Jun 2009 A1
20090286383 Jiang et al. Nov 2009 A1
20100000762 Yang et al. Jan 2010 A1
20100035375 Grigoropoulos et al. Feb 2010 A1
20110043965 Yaniv et al. Feb 2011 A1
Foreign Referenced Citations (38)
Number Date Country
1509206 Jun 2004 CN
1803940 Jul 2006 CN
101065203 Oct 2007 CN
101116149 Jan 2008 CN
1626106 Feb 2006 EP
1626106 Aug 2006 EP
1758166 Feb 2007 EP
2045028 Apr 2009 EP
2150417 Feb 2010 EP
1758166 Sep 2011 EP
62124084 Jun 1987 JP
10-308119 Nov 1998 JP
11-319538 Nov 1999 JP
2001-325831 Nov 2001 JP
2003-292836 Oct 2003 JP
2004-127676 Apr 2004 JP
2004-273592 Sep 2004 JP
2005-307335 Nov 2005 JP
2006-026602 Feb 2006 JP
2006-169592 Jun 2006 JP
2006-186330 Jul 2006 JP
2006-229212 Aug 2006 JP
2006-321948 Nov 2006 JP
2007-042725 Feb 2007 JP
2007-321215 Dec 2007 JP
2007-327058 Dec 2007 JP
2007-332347 Dec 2007 JP
2008006513 Jan 2008 JP
2009-097082 May 2009 JP
9708924 Mar 1997 WO
03106573 Dec 2003 WO
2004005413 Jan 2004 WO
2006072959 Jul 2006 WO
2006076603 Jul 2006 WO
2007004033 Jan 2007 WO
2007013393 Feb 2007 WO
2008144504 Nov 2008 WO
2009111393 Sep 2009 WO
Non-Patent Literature Citations (78)
Entry
Schroder et al., “Broadcast Photonic Curing of Metallic Nanoparticle Films,” Nanotechnologies, Inc. publication, 2006 NSTI Nanotechnology Conference and Trade Show, May 7-11, 2006, 4 pages.
Lu et al., “Ultrahigh Strength and High Electrical Conductivity in Copper,” Science Magazine, Apr. 2004, vol. 304, 6 pages.
Volkman et al., “Ink-jetted Silver/Copper Conductors for printed RFID Applications,” Materials Research Society Magazine, 2004, vol. 814, 6 pages.
Wu et al., “One-Step Green Route to Narrowly Dispersed Copper Nanocrystals,” Journal of Nanoparticle Research, 2006, pp. 965-969, 5 pages.
Curtis et al., “Spray and Inkjet Printing of Hybrid Nanoparticle-Metal-Organic Inks for Ag and Chu Metallizations,” Materials Research Society Magazine, 2001, vol. 676, 6 pages.
Shacham-Diamand, “Electroless Copper Deposition Using Glyoxylic Acid as Reducing Agent for Ultralarge Scale Integration Metallization,” manuscript published by Electrochemical and Solid-State Letters, Apr. 2000, pp. 279-282, 4 pages.
Yeshchenko et al., “Size-Dependent Melting of Spherical Copper Nanoparticles,” article published by National Tams Shevchenko Kyiv University, Jan. 2007, 16 pages.
Shah et al., “Trimming and Printing of Embedded Resistors Using Demand-Mode Ink-Jet Technology and Conductive Polymer,” IPC Printed Circuit Expo Mar. 24-28, 2002, pp. 1-5.
International Searching Authority, International Search Report and the Written Opinion, PCT/US08/63890, Aug. 6, 2008, 9 pages.
International Searching Authority, International Search Report and Written Opinion for Application No. PCT/US/09/35717, May 5, 2009, 7 pages.
Niizeki et al., “Laser Sintering of Ag Nanopaste Film and Its Application to Bond-Pad Formation,” 2008 Electronic Components and Technology Conference, May 27-30, 2008, IEEE, pp. 1745-1750.
Lee et al, “Spontaneous Growth Mechanism of Tin Whsker,” Acta mater vol. 46, No. 10, pp. 3701-3714, 1998.
Galyon, “Annotated Tin Whisker Bibliography and Anthology,” IEEE Transactions on Electronics Packaging Manufacturing, vol. 28, No. 1, Jan. 2005, pp. 94-122.
Lal et al., “Role of Intrinsic Stresses in the Phenomena of Tin Whiskers in Electrical Connectors,” IEEE Transactions on Electronics Packing Manufacturing, vol. 28, No. 1, Jan. 2005, pp. 63-74.
Boettinger et al., “Whisker and Hillock Formation on Sn, Sn—Cu and Sn—Pb Electrodeposits,” Acta Materialia, 53, Sep. 8, 2005, pp. 5033-5050.
Mitooka et al., “Effect of Laser Irradiation on Generation Growth of Whiskers in Tin-Electroplated Film,” J. Japan Inst. Metals, vol. 73, No. 3, (2009), pp. 226-233.
Osenbach et al., “Sn Corrosion and Its Influence on Whisker Growth,” IEEE Transactions on Electronic Packaging Manufacturing, vol. 30, No. 1, Jan. 2007, pp. 23-35.
Osenbach et al., “Sn Whiskers: Material, Design, Processing, and Post-Plate Reflow Effects and Development of an Overall Phenomenological Theory,” IEEE Transactions on Electronics Packaging Manufacturing, vol. 28, No. 1, Jan. 2005, pp. 36-62.
Osterman, “Mitigation Strategies for Tin Whiskers,” Release 1.0, Aug. 28, 2002, 11 pages.
Schroeder et al., “Tin Whisker Test Method Development,” IEEE Transactions Electronics Packaging Manufacturing, vol. 29, No. 4, Oct. 2006, pp. 231-238.
International Searching Authority, International Search Report and Written Opinion for International Application No. PCT/US09/44196, Jun. 30, 2009, 8 pages.
International Searching Authority, International Search Report and Written Opinion for International Application No. PCT/US09/44195, Jun. 25, 2009, 7 pages.
International Preliminary Report on Patentability, International Application No. PCT/US2009/044196, Nov. 25, 2010, 6 pages.
International Preliminary Report on Patentability, International Application No. PCT/US2009/044195, Nov. 25, 2010, 5 pages.
International Searching Authority, International Search Report and Written Opinion for International Application No. PCT/US09/49510, Oct. 19, 2009.
International Preliminary Report on Patentability, PCT/US2008/063890, Dec. 3, 2009.
International Searching Authority, International Search Report and Written Opinion of the International Searching Authority for PCT/US10/28799, May 19, 2010.
International Searching Authority, International Search Report and the Written Opinion for International Application No. PCT/US10/28811, May 18, 2010.
MSDS: Fluorad by 3M, Fluorosurfactant FC-4430, Mar. 2, 2002; www.3m.com/paintsandcoatings, 4 pages.
European Patent Office, Supplemental European Search Report for Application No. EP 09774505, Jun. 29, 2011.
The State Intellectual Property Office of The People's Republic of China, Notice of the First Office Action, Application No. 200880021733.6, Jun. 22, 2011.
European Patent Office, Supplementary European Search Report for Application No. EP08755692, Aug. 6, 2010.
Kogelschatz, “Excimer Lamps: History, Discharge Physics, and Industrial Applications”, Proc. SPIE, vol. 5483, 2004, pp. 272-286.
Kim et al., “Cyclic Properties of Si—Cu/Carbon Nanocomposite Anodes for Li-Ion Secondary Batteries”, Journal of the Electrochemical Society, vol. 152, No. 3, pp. A-523-A-526, Jan. 24, 2005, retrieved from internet Aug. 26, 2010.
International Searching Authority, International Search Report and the Written Opinion for PCT/US10/042169, mailed on Sep. 7, 2010, 4 pages.
Yaniv, “Novel Inkettable Copper Ink Utilizing Processing Temperatures Under 100 Degrees C Without the Need of Inert Atmosphere”, Presentation at Printed Electronics Europe Conference, pp. 1-25, Apr. 7-8, 2009, retrieved from internet Aug. 26, 2010.
The International Bureau of WIPO, International Preliminary Report on Patentability for PCT/US2010/042169, Jan. 17, 2012.
The State Intellectual Property Office of The People's Republic of China, Notice on the First Office Action; Patent Application No. 200980108344.1, Jan. 21, 2012.
European Patent Office, Examination Report, Application No. 08 755 692.4, Apr. 13, 2012.
Champion at al., “Sintering of copper nanopowders under hydrogen: an in situ X-ray diffraction analysis,” Materials Science and Engineering A, vol. 360, No. 1-2, Nov. 1, 2003, pp. 258-263.
The State Intellectual Property Office of The People's Republic of China, Notice on Grant of Patent Right for Invention, Application No. 200880021733.6, Apr. 20, 2012.
The State Intellectual Property Office of The People's Republic of China, Notice on the First Office Action, Application No. 200980125925.6, Mar. 31, 2012, 8 pages, CN.
Korean Intellectual Property Office, Chemistry & Biotechnology Examination Bureau, Notice to File a Response, Patent Application No. 10-2010-7022240, May 8, 2012, KR.
Tego 425 Flow Datasheet; http://evonik.tego.de/pdf/daten/amer/Flow—425.pdf.
United States Patent & Trademark Office, Final Office Action Summary, U.S. Appl. No. 12/391,817, dated Aug. 27, 2012.
United States Patent & Trademark Office, Non-Final Office Action Summary, U.S. Appl. No. 12/496,453, dated Jun. 13, 2012.
European Patent Office, Examination Report, Application No. 09774505.3, dated Sep. 26, 2012.
United States Patent & Trademark Office, Non-Final Office Action, U.S. Appl. No. 12/466,306, dated Nov. 7, 2012.
Japanese Patent Office, Non-Final Office Action, Japanese Patent Application No. 2011-509765, Jul. 23, 2013.
The State Intellectual Property Office of The People's Republic of China, Application No. 200980118341.6, Notice on the First Office Action, Feb. 17, 2013.
United States Patent & Trademark Office, Non-Final Office Action, Application No. 13/260,893, Mar. 11, 2013.
Translation of Office Action and Taiwan IPO Search Report, Taiwan Invention Patent Application No. 0977118130, May 31, 2013.
The State Intellectual Property Office of The People's Republic of China, Notice on the Second Office Action and Search Report, Patent Application No. 200980108344.1, Dec. 5, 2012.
Korean Intellectual Property Office, Notice of Reasons for Rejection, Application No. 2010-549783, Dec. 18, 2012.
The State Intellectual Property Office of The People's Republic of China, Notice on the Second Office Action, Application No. 200980125925.6, Feb. 25, 2013, 11 pages, CN.
Translated Text of First Office Action for Application No. 201080015842.4, May 6, 2013, 6 pages, CN.
Non-Final Office Action, Notice of Reasons for Rejection, Japanese Patent Application No. 2012-502281, mailed Jul. 16, 2013,.
The State Intellectual Property Office of The People's Republic of China, Notice on the First Office Action, Application No. 20108002385E8, Jul. 15, 2013, 8 pages, CN.
Translation of Notice of Reasons for Rejection, Japanese Patent Application No. 2011-516873, Oct. 22, 2013.
The State Intellectual Property Office of The People's Republic of China, Notice on the First Office Action, Application No. 201080032626.0, Jun. 28, 2013, 7 pages, CN.
The State Intellectual Property Office of The People's Republic of China, Notice on the Third Office Action, Application No. 200980125925.6, Nov. 5, 2013, 1 page, CN.
Japanese Patent Office, Final Office Action, Notice of Reasons for Rejection, Japanese Patent Application No. 2010-549783, dated Oct. 15, 2013.
Japanese Patent Office, Non-Final Office Action, Notice of Reasons for Rejection, Japanese Patent Application No. 2012-503530, dated Jan. 21, 2014.
The State Intellectual Property Office of The People's Republic of China, Notice on the Third Office Action; Patent Application No. 200980108344.1, Feb. 27, 2014, English Translation.
The State Intellectual Property Office of The People's Republic of China, Translated text of Notice on the Second Office Action; Patent Application No. 201080015842.4, Mar. 10, 2014.
Japanese Patent Office, Non-Final Office Action, Notice of Reasons for Rejection, Japanese Patent Application No. 2011-516873, dated Mar. 24, 2014.
The State Intellectual Property Office of The People's Republic of China, Notice on the Second Office Action; Patent Application No. 201080023851.8, Apr. 8, 2014, CN.
European Patent Office, European Search Report, Application No. 09747709.5, dated Mar. 12, 2014.
The State Intellectual Property Office of The People's Republic of China, Notice on the Second Office Action; Patent Application No. 201080032626.0, Apr. 16, 2014.
European Patent Office, European Search Report for International Application No. 10756901.4, dated Oct. 10, 2014.
Japanese Patent Office, Decision on Rejection, Japanese Patent Application No. 2011-509765, Sep. 29, 2014.
European Patent Office, European Search Report, Application No. 10759242.0, dated Sep. 3, 2014.
Japanese Patent Office, Final Office Action, Notice of Reasons for Rejection, Japanese Patent Application No. 2010-549783, dated Oct. 14, 2014.
European Patent Office, Examination Report, Application No. 09774505.3, dated Oct. 22, 2014.
Taiwan International Patent & Law Office, Translation of Notice of Office Action and Search Report, Taiwan Invention Patent Application No. 099109236, dated Oct. 23, 2014.
The State Intellectual Property Office of the People's Republic of China, Text of the Third Office Action; Patent Application No. 201080015842.4, Sep. 5, 2014.
Taiwan International Patent & Law Office, Translation of Notice of Office Action and Search Report, Taiwan Invention Patent Application No. 098116219, dated Oct. 15, 2014.
Japanese Patent Office, Final Office Action, Notice of Reasons for Rejection, Japanese Patent Application No. 2012-502281, dated Aug. 11, 2014.
Related Publications (1)
Number Date Country
20140057428 A1 Feb 2014 US
Provisional Applications (2)
Number Date Country
61174758 May 2009 US
61163894 Mar 2009 US
Continuations (1)
Number Date Country
Parent 13260893 US
Child 14073986 US