This disclosure relates to lead-free solder, and more particularly, to a semiconductor device and a semiconductor assembly using the lead-free solder.
Modern integrated circuits are made up of literally millions of active devices such as transistors and capacitors. These devices are initially isolated from each other, but are later interconnected together to form functional circuits. Typical interconnect structures include lateral interconnections, such as metal lines (wirings), and vertical interconnections, such as vias and contacts. Interconnections are increasingly determining the limits of performance and the density of modern integrated circuits. On top of the interconnect structures, bond pads are formed and exposed on the surface of the respective chip. Electrical connections are made through bond pads to connect the chip to a package substrate or another die. Bond pads can be used for wire bonding or flip-chip bonding. Wafer level chip scale packaging (WLCSP) is currently widely used for its low cost and relatively simple processes. In a typical WLCSP, interconnect structures are formed on metallization layers, followed by the formation of under-bump metallurgy (UBM), and the mounting of solder balls.
Flip-chip packaging utilizes bumps to establish electrical contact between a chip's I/O pads and the substrate or lead frame of the package. Structurally, a bump actually contains the bump itself and a so-called under bump metallurgy (UBM) located between the bump and an I/O pad. An UBM generally contains an adhesion layer, a barrier layer and a wetting layer, arranged in this order on the I/O pad. The bumps themselves, based on the material used, are classified as solder bumps, gold bumps, copper pillar bumps and bumps with mixed metals. Recently, copper interconnect post technology is proposed. Instead of using solder bump, the electronic component is connected to a substrate by means of copper post. The copper interconnect post technology achieves finer pitch with minimum probability of bump bridging, reduces the capacitance load for the circuits and allows the electronic component to perform at higher frequencies. A solder alloy is still necessary for capping the bump structure and jointing electronic components as well.
Usually, a material used for the solder alloy is so-called Sn—Pb eutectic solder of Sn-38 mass % Pb. In recent years, it is urged to put Pb-free solder to practical use. The binary Sn—Ag alloy is used as the lead-free solder with Ag between 2.0˜4.5 weight percent, which melts at a temperature between 240˜260° C. The reflow soldering process and equipment for lead-free components are similar to conventional eutectic solder. Many developments of solder alloys have been directed to make the composition of an alloy, as close as possible to the eutectic composition of that in order to use the eutectic point to avoid thermal damage. However, the melting point of a Pb-free solder material is higher than that of the conventional Sn—Pb eutectic solder, so that there arises problems of cracks and stress reliability issues as TCB testing, especially to large die size. Even applied to the Cu post technology, the flip-chip assembly using the Pb-free solder material as the cap still suffers the crack issue induced by die edge/substrate interface stress.
The aforementioned objects, features and advantages of this disclosure will become apparent by referring to the following detailed description of the preferred embodiments with reference to the accompanying drawings, wherein:
This disclosure provides a lead-free solder with controlled Ag content and reflow temperature used in semiconductor devices having Cu post, post passivation interconnects, solder bump, and/or through-silicon vias (TSVs) fabricated thereon, applied to flip-chip assembly, wafer-level chip scale package (WLCSP), three-dimensional integrated circuit (3D-IC) stack, and/or any advanced package technology fields. In the following description, numerous specific details are set forth to provide a thorough understanding of the disclosure. However, one having an ordinary skill in the art will recognize that the disclosure can be practiced without these specific details. In some instances, well-known structures and processes have not been described in detail to avoid unnecessarily obscuring the disclosure. Reference throughout this specification to “one embodiment” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment. Thus, the appearances of the phrases “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily all referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments. It should be appreciated that the following figures are not drawn to scale; rather, these figures are merely intended for illustration.
Herein, cross-sectional diagram of
An example of a substrate 10 used for Cu post interconnection fabrication may comprise a semiconductor substrate as employed in a semiconductor integrated circuit fabrication, and integrated circuits may be formed therein and/or thereupon. The semiconductor substrate is defined to mean any construction comprising semiconductor materials, including, but is not limited to, bulk silicon, a semiconductor wafer, a silicon-on-insulator (SOI) substrate, or a silicon germanium substrate. Other semiconductor materials including group III, group IV, and group V elements may also be used. The integrated circuits as used herein refer to electronic circuits having multiple individual circuit elements, such as transistors, diodes, resistors, capacitors, inductors, and other active and passive semiconductor devices. The substrate 10 further includes inter-layer dielectric layers and a metallization structure overlying the integrated circuits. The inter-layer dielectric layers in the metallization structure include low-k dielectric materials, un-doped silicate glass (USG), silicon nitride, silicon oxynitride, or other commonly used materials. The dielectric constants (k value) of the low-k dielectric materials may be less than about 3.9, or less than about 2.8. Metal lines in the metallization structure may be formed of copper or copper alloys. One skilled in the art will realize the formation details of the metallization layers.
A conductive region 12 is a top metallization layer formed in a top-level inter-layer dielectric layer, which is a portion of conductive routs and has an exposed surface treated by a planarization process, such as chemical mechanical polishing (CMP), if necessary. Suitable materials for the conductive region 12 may include, but are not limited to, for example copper, aluminum, copper alloy, or other mobile conductive materials. In one embodiment, the conductive region 12 is a pad region 12, which may be used in the bonding process to connect the integrated circuits in the respective chip to external features.
A passivation layer 14 is formed and patterned on the substrate 10 to partially cover the pad region 12. The passivation layer 14 has an opening 15 exposing a portion of the pad region 12. The passivation layer 14 may be formed of a non-organic material selected from un-doped silicate glass (USG), silicon nitride, silicon oxynitride, silicon oxide, and combinations thereof. Alternatively, the passivation layer 14 may be formed of a polymer layer, such as an epoxy, polyimide, benzocyclobutene (BCB), polybenzoxazole (PBO), and the like, although other relatively soft, often organic, dielectric materials may also be used.
An under-bump-metallurgy (UBM) layer 16 including a diffusion barrier layer 16a and a seed layer 16b is formed on a portion of the passivation layer 14 and electrically connected to the pad region 12 through the opening 15. As depicted, the UBM layer 28 directly contacts the exposed portion of the pad region 12 and lines the sidewalls and bottom of the opening 15. The diffusion barrier layer 16a, also referred to as a glue layer, is formed to cover the sidewalls and the bottom of the opening 15. The diffusion barrier layer 16a may be formed of tantalum nitride, although it may also be formed of other materials such as titanium nitride, tantalum, titanium, or the like. The formation methods include physical vapor deposition (PVD) or sputtering. The seed layer 16b may be a copper seed layer formed on the diffusion barrier layer 16a. The seed layer 16b may be formed of copper alloys that include silver, chromium, nickel, tin, gold, and combinations thereof. In one embodiment, the UBM layer 16 is a Cu/Ti layer.
A copper (Cu) post 18 is formed on the UBM layer 16. As used throughout this disclosure, the term “copper (Cu) post” is intended to include substantially a post including pure elemental copper, copper containing unavoidable impurities, and copper alloys containing minor amounts of elements such as tantalum, indium, tin, zinc, manganese, chromium, titanium, germanium, strontium, platinum, magnesium, aluminum or zirconium. The formation methods may include sputtering, printing, electro plating, electroless plating, and commonly used chemical vapor deposition (CVD) methods. For example, electro-chemical plating (ECP) is carried out to form the Cu post with a thickness greater than 40 um. In other embodiments, the thickness of the Cu post is about 40˜70 μm, although the thickness may be greater or smaller.
A cap layer 20 is formed on the top surface of the Cu post 18. The cap layer 20 could act as a barrier layer to prevent copper in the Cu post 18 to diffuse into bonding material, such as solder alloy, that is used to bond the substrate 10 to external features. The prevention of copper diffusion increases the reliability and bonding strength of the package. The cap layer 20 may include nickel, tin, tin-lead (SnPb), gold (Au), silver, palladium (Pd), In, nickel-palladium-gold (NiPdAu), nickel-gold (NiAu), other similar materials, or alloy. In one embodiment, the cap layer 20 is a nickel layer with a thickness about 1˜5 um.
A lead-free (Pb-free) solder layer 22 is formed on the cap layer 20. Thus the lead-free solder layer 22, the cap layer 20, and the Co post 18 are referred to as a bump structure 25 formed over the pad region 12. The lead-free (Pb-free) solder layer 22 may be formed by plating and reflowing processes. In one embodiment, the lead-free solder layer 22 is formed as solder ball on the cap layer 20. In other embodiment, the lead-free solder layer 22 is a plated solder layer on the cap layer 20. For a lead-free solder system, the solder layer 22 is SnAg with Ag content being controlled lower than 1.6 weight percent (wt %). In the reflow process, the melting temperature of the lead-free solder layer 22 is accordingly adjusted to the range of between about 240° C. to about 280° C. In one embodiment, the Ag content in the lead-free solder layer 22 is at the range between about 1.2 wt % to about 1.6 wt %. In other embodiment, the Ag content in the lead-free solder layer 22 is about 1.5 wt %. Reliability of package using lead-free solder alloy relates to several factors, including bump hardness and formation of intermetallic compounds (IMCs) and voids, which may potentially contribute to crack formation and cause thermo-mechanical stresses on the solder joint. It is observed that the bump becomes softer as the Ag content in the lead-free solder is lower as schematically shown in
The substrate 10 may then be sawed and packaged onto a package substrate, or another die, with solder balls or Cu posts mounted on a pad on the package substrate or the other die. The structure shown in
Compared with the Cu post 18 and the UBM layer 16 formed over the pad region 12 as depicted in
Compared with the structure as depicted in
Referring to
A first dielectric layer 214 is formed on the first surface 10a, in which contacts are formed to electrically connect the devices respectively. Generally, the first dielectric layer 214 may be formed, for example, of a low-K dielectric material, silicon oxide, phosphosilicate glass (PSG), borophosphosilicate glass (BPSG), fluorinated silicate glass (FSG), or the like, by any suitable method known in the art. Other materials and processes may be used.
A plurality of through vias 216 passes through at least a part of the substrate 210. The through via 216 is a conductor-filled plug extending from the first surface 210a toward the second surface 10b and reaching an intended depth. Also, an isolation layer is formed on the sidewalls and bottom of the though via 216, and insulates the though via 216 from the substrate 210. The through vias 16 may be formed of any suitable conductive material, but are preferably formed of a highly-conductive, low-resistive metal, elemental metal, transition metal, or the like. In an embodiment, the though via 216 is a trench filled with a conductive layer formed of Cu, W, Cu alloy, or the like. A conductive barrier layer formed of Ti, TiN, Ta, TaN or combinations thereof may be formed in the trench surrounding the conductive layer. The isolation layer may be formed of commonly used dielectric materials such as silicon nitride, silicon oxide (for example, tetra-ethyl-ortho-silicate (TEOS) oxide), and the like.
A first interconnect structure 218, which includes inter-layer dielectric layers and a metallization structure are formed overlying the integrated circuits, the first dielectric layer 214 and the through vias 216. The inter-layer dielectric layers in the metallization structure include low-k dielectric materials, un-doped silicate glass (USG), silicon nitride, silicon oxynitride, or other commonly used materials. The dielectric constants (k value) of the low-k dielectric materials may be less than about 3.9, or less than about 2.8. The metallization structure includes metal lines and vias, which may be formed of copper or copper alloys, and may be formed using the well-known damascene processes. One skilled in the art will realize the formation details of the metallization layers.
A passivation layer 220 is formed over first interconnect structure 218. The passivation layer 220 may be formed of materials such as silicon oxide, silicon nitride, un-doped silicate glass (USG), polyimide, and/or multi-layers thereof. A metal pad 222 is formed on the passivation layer 220. The metal pad 222 may be formed of aluminum, copper, silver, gold, nickel, tungsten, alloys thereof, and/or multi-layers thereof. The metal pad may be electrically connected to the devices and the through via 216, for example, through underlying first interconnection structure 218. A dielectric buffer layer 224 is formed on the metal pad and patterned to provide a bump formation window. The dielectric buffer layer 224 may be formed of a polymer, such as an epoxy, polyimide, benzocyclobutene (BCB), polybenzoxazole (PBO), and the like, although other relatively soft, often organic, dielectric materials can also be used. A bump structure 226 is then formed overlying and electrically connected to the metal pad 222. The bump structure 224 refers to the structures 25 and 25a shown in
Referring to
Next, dies 400 are provided for being bonded onto the thinned wafer 210″. The dies 400 may be memory chips, RF (radio frequency) chips, logic chips, or other chips. Each die 400 includes a bump structure 402 used for electrically connected to the second interconnect structure 228 of the thinned wafer 210″. The bump structure 402 includes a copper layer 404, an optional cap layer 406 on the top of the copper layer 404, and a lead-free solder layer 408 over the copper layer 404. The copper layer 404 may be a thin copper layer of about 0.5˜10 um thickness or a thick copper layer of about 40˜70 μm thickness. The optional cap layer 406 may include nickel, gold (Au), silver, palladium (Pd), indium (In), nickel-palladium-gold (NiPdAu), nickel-gold (NiAu) or other similar materials or alloy. The lead-free solder layer 408 may be a plated layer or reflowed as a solder ball. The solder layer 408 is SnAg with Ag content being controlled lower than 1.6 weight percent (wt %). In the reflow process, the melting temperature of the lead-free solder layer 408 is accordingly adjusted to the range of between about 240° C. to about 280° C. In one embodiment, the Ag content in the lead-free solder layer 408 is at the range between about 1.2 wt % to about 1.6 wt %. In other embodiment, the Ag content in the lead-free solder layer 408 is about 1.5 wt %.
Referring to
In the preceding detailed description, the disclosure is described with reference to specifically exemplary embodiments thereof. It will, however, be evident that various modifications, structures, processes, and changes may be made thereto without departing from the broader spirit and scope of the disclosure, as set forth in the claims. The specification and drawings are, accordingly, to be regarded as illustrative and not restrictive. It is understood that the disclosure is capable of using various other combinations and environments and is capable of changes or modifications within the scope of the inventive concept as expressed herein.
Number | Name | Date | Kind |
---|---|---|---|
3528090 | Van Laer | Sep 1970 | A |
4380867 | Antson | Apr 1983 | A |
4720740 | Clements et al. | Jan 1988 | A |
4811082 | Jacobs et al. | Mar 1989 | A |
4990462 | Sliwa, Jr. | Feb 1991 | A |
5075253 | Sliwa, Jr. | Dec 1991 | A |
5134460 | Brady et al. | Jul 1992 | A |
5380681 | Hsu | Jan 1995 | A |
5391917 | Gilmour et al. | Feb 1995 | A |
5448114 | Kondoh et al. | Sep 1995 | A |
5481133 | Hsu | Jan 1996 | A |
5510298 | Redwine | Apr 1996 | A |
5747881 | Hosomi et al. | May 1998 | A |
5767001 | Bertagnolli et al. | Jun 1998 | A |
5998292 | Black et al. | Dec 1999 | A |
6002177 | Gaynes et al. | Dec 1999 | A |
6184060 | Siniaguine | Feb 2001 | B1 |
6187678 | Gaynes et al. | Feb 2001 | B1 |
6191493 | Yasunaga et al. | Feb 2001 | B1 |
6218281 | Watanabe et al. | Apr 2001 | B1 |
6229216 | Ma et al. | May 2001 | B1 |
6229220 | Saitoh et al. | May 2001 | B1 |
6232563 | Kim et al. | May 2001 | B1 |
6236115 | Gaynes et al. | May 2001 | B1 |
6271059 | Bertin et al. | Aug 2001 | B1 |
6279815 | Correia et al. | Aug 2001 | B1 |
6322903 | Siniaguine et al. | Nov 2001 | B1 |
6355501 | Fung et al. | Mar 2002 | B1 |
6426556 | Lin | Jul 2002 | B1 |
6434016 | Zeng et al. | Aug 2002 | B2 |
6448168 | Rao et al. | Sep 2002 | B1 |
6448661 | Kim et al. | Sep 2002 | B1 |
6461895 | Liang et al. | Oct 2002 | B1 |
6464895 | Forat et al. | Oct 2002 | B2 |
6465892 | Suga | Oct 2002 | B1 |
6472293 | Suga | Oct 2002 | B1 |
6492198 | Hwang | Dec 2002 | B2 |
6538333 | Kong | Mar 2003 | B2 |
6562653 | Ma et al. | May 2003 | B1 |
6570248 | Ahn et al. | May 2003 | B1 |
6576381 | Hirano et al. | Jun 2003 | B1 |
6578754 | Tung | Jun 2003 | B1 |
6590295 | Liao et al. | Jul 2003 | B1 |
6592019 | Tung | Jul 2003 | B2 |
6599778 | Pogge et al. | Jul 2003 | B2 |
6600222 | Levardo | Jul 2003 | B1 |
6607938 | Kwon et al. | Aug 2003 | B2 |
6639303 | Siniaguine | Oct 2003 | B2 |
6661085 | Kellar et al. | Dec 2003 | B2 |
6664129 | Siniaguine | Dec 2003 | B2 |
6693361 | Siniaguine et al. | Feb 2004 | B1 |
6731003 | Joshi et al. | May 2004 | B2 |
6740582 | Siniaguine | May 2004 | B2 |
6762076 | Kim et al. | Jul 2004 | B2 |
6770958 | Wang et al. | Aug 2004 | B2 |
6790748 | Kim et al. | Sep 2004 | B2 |
6800930 | Jackson et al. | Oct 2004 | B2 |
6818545 | Lee et al. | Nov 2004 | B2 |
6828677 | Yap et al. | Dec 2004 | B2 |
6841883 | Farnworth et al. | Jan 2005 | B1 |
6853076 | Datta et al. | Feb 2005 | B2 |
6869831 | Cowens et al. | Mar 2005 | B2 |
6879041 | Yamamoto et al. | Apr 2005 | B2 |
6882030 | Siniaguine | Apr 2005 | B2 |
6887769 | Kellar et al. | May 2005 | B2 |
6908565 | Kim et al. | Jun 2005 | B2 |
6908785 | Kim | Jun 2005 | B2 |
6917119 | Lee et al. | Jul 2005 | B2 |
6924551 | Rumer et al. | Aug 2005 | B2 |
6943067 | Greenlaw | Sep 2005 | B2 |
6946384 | Kloster et al. | Sep 2005 | B2 |
6958539 | Lay et al. | Oct 2005 | B2 |
6962867 | Jackson et al. | Nov 2005 | B2 |
6962872 | Chudzik et al. | Nov 2005 | B2 |
6975016 | Kellar et al. | Dec 2005 | B2 |
7008867 | Lei | Mar 2006 | B2 |
7012333 | Shimoyama et al. | Mar 2006 | B2 |
7030481 | Chudzik et al. | Apr 2006 | B2 |
7037804 | Kellar et al. | May 2006 | B2 |
7049170 | Savastiouk et al. | May 2006 | B2 |
7056807 | Kellar et al. | Jun 2006 | B2 |
7060601 | Savastiouk et al. | Jun 2006 | B2 |
7064436 | Ishiguri et al. | Jun 2006 | B2 |
7071546 | Fey et al. | Jul 2006 | B2 |
7087538 | Staines et al. | Aug 2006 | B2 |
7111149 | Eilert | Sep 2006 | B2 |
7122912 | Matsui | Oct 2006 | B2 |
7151009 | Kim et al. | Dec 2006 | B2 |
7157787 | Kim et al. | Jan 2007 | B2 |
7193308 | Matsui | Mar 2007 | B2 |
7215033 | Lee et al. | May 2007 | B2 |
7262495 | Chen et al. | Aug 2007 | B2 |
7271497 | Joshi et al. | Sep 2007 | B2 |
7276799 | Lee et al. | Oct 2007 | B2 |
7279795 | Periaman et al. | Oct 2007 | B2 |
7297574 | Thomas et al. | Nov 2007 | B2 |
7307005 | Kobrinsky et al. | Dec 2007 | B2 |
7317256 | Williams et al. | Jan 2008 | B2 |
7320928 | Kloster et al. | Jan 2008 | B2 |
7335972 | Chanchani | Feb 2008 | B2 |
7345350 | Sinha | Mar 2008 | B2 |
7348210 | Daubenspeck et al. | Mar 2008 | B2 |
7355273 | Jackson et al. | Apr 2008 | B2 |
7391112 | Li et al. | Jun 2008 | B2 |
7402442 | Condorelli et al. | Jul 2008 | B2 |
7402515 | Arana et al. | Jul 2008 | B2 |
7410884 | Ramanathan et al. | Aug 2008 | B2 |
7432592 | Shi et al. | Oct 2008 | B2 |
7462942 | Tan et al. | Dec 2008 | B2 |
7494845 | Hwang et al. | Feb 2009 | B2 |
7501311 | Tsai | Mar 2009 | B2 |
7524755 | Widodo et al. | Apr 2009 | B2 |
7528494 | Furukawa et al. | May 2009 | B2 |
7531890 | Kim | May 2009 | B2 |
7557597 | Anderson et al. | Jul 2009 | B2 |
7566650 | Lin et al. | Jul 2009 | B2 |
7576435 | Chao | Aug 2009 | B2 |
7592246 | Akram | Sep 2009 | B2 |
7648899 | Banerji et al. | Jan 2010 | B1 |
7825511 | Daubenspeck et al. | Nov 2010 | B2 |
7834450 | Kang | Nov 2010 | B2 |
7928534 | Hsu et al. | Apr 2011 | B2 |
20010000321 | Takeda et al. | Apr 2001 | A1 |
20020014705 | Ishio et al. | Feb 2002 | A1 |
20020033531 | Matsushima et al. | Mar 2002 | A1 |
20030156969 | Choi et al. | Aug 2003 | A1 |
20030216025 | Lu et al. | Nov 2003 | A1 |
20040166661 | Lei | Aug 2004 | A1 |
20050001324 | Dunn et al. | Jan 2005 | A1 |
20050077624 | Tan et al. | Apr 2005 | A1 |
20050179131 | Homma | Aug 2005 | A1 |
20060017160 | Huang | Jan 2006 | A1 |
20060043603 | Ranade et al. | Mar 2006 | A1 |
20060166402 | Lim et al. | Jul 2006 | A1 |
20060237842 | Shindo | Oct 2006 | A1 |
20060278982 | Solo | Dec 2006 | A1 |
20070023904 | Salmon | Feb 2007 | A1 |
20070080451 | Suh | Apr 2007 | A1 |
20070108606 | Watanabe | May 2007 | A1 |
20070284684 | Naito et al. | Dec 2007 | A1 |
20070287279 | Daubenspeck et al. | Dec 2007 | A1 |
20080296764 | Chang et al. | Dec 2008 | A1 |
20090011543 | Karta et al. | Jan 2009 | A1 |
20090026608 | Tsai et al. | Jan 2009 | A1 |
20090045511 | Meyer et al. | Feb 2009 | A1 |
20090096109 | Iwasaki | Apr 2009 | A1 |
20090098724 | Yu | Apr 2009 | A1 |
20090130840 | Wang et al. | May 2009 | A1 |
20090197114 | Shih et al. | Aug 2009 | A1 |
20090229857 | Fredenberg et al. | Sep 2009 | A1 |
20100090318 | Hsu et al. | Apr 2010 | A1 |
20100109159 | Ho et al. | May 2010 | A1 |
20100230810 | Kang et al. | Sep 2010 | A1 |
20110101523 | Hwang et al. | May 2011 | A1 |
20110101526 | Hsiao et al. | May 2011 | A1 |
20110156256 | Kang et al. | Jun 2011 | A1 |
20110227216 | Tseng et al. | Sep 2011 | A1 |
20110281432 | Farooq et al. | Nov 2011 | A1 |
Number | Date | Country |
---|---|---|
1606155 | Apr 2005 | CN |
1993335313 | Dec 1993 | JP |
2000228420 | Aug 2000 | JP |
502424 | Sep 2002 | TW |
200828548 | Oct 2007 | TW |
200908173 | Feb 2009 | TW |
200947509 | Nov 2009 | TW |
Entry |
---|
Kim, K. S., et al., “The Interface Formation and Adhesion of Metals (Cu, Ta, and Ti) and Low Dielectric Constant Polymer-Like Organic Thin Films Deposited by Plasma-Enhanced Chemical Vapor Deposition Using Para-Xylene Precursor”, Thin Solid Films 377-378 (2000), pp. 122-128. |
Kim, K. J., et al., “Chemical Interaction, Adhesion and Diffusion Properties at the Interface of Cu and Plasma-Treated Thiophene-Based Plasma Polymer (ThioPP) Films”, Thin Solid Films 398-399 (2001), pp. 657-662. |
Du, M., et al., “The Interface Formation of Copper and Low Dielectric Constant Fluoro-Polymer: Plasma Surface Modification and its Effect on Copper Diffusion”, Journal of Applied Physics, vol. 85, No. 3, Feb. 1, 1999, pp. 1496-1502. |
Jiang, Liang-You, et al., “Reduced Copper Diffusion in Layered Silicate/Fluorinated Polyimide (6FDS-ODA) Nanocomposites”, Journal of Applied Polymer Science, vol. 92, 1422-1425 (2004). |
U.S. Appl. No. 61/258,414, filed Nov. 5, 2009, Chien Ling Hwang, et al. |
U.S. Appl. No. 61/238,749, filed Sep. 1, 2009, Chung-Shi Liu. |
U.S. Appl. No. 61/258,393, filed Nov. 5, 2009, Chien Ling Hwang, et al. |
U.S. Appl. No. 61/230,012, filed Jul. 30, 2009, Chung-Shi Liu, et al. |
Chinese Office Action in Corresponding Application No. 201010213358.4. |
Office Action dated Sep. 27, 2013 from corresponding application No. TW 099118671. |
Number | Date | Country | |
---|---|---|---|
20110193219 A1 | Aug 2011 | US |