The present application is related to U.S. provisional Application No. 61/258,393, entitled “Copper Pillar Bump with Barrier Layer for Reducing The Thickness of Intermetallic Compound,” filed on Nov. 5, 2009, and U.S. application Ser. No. 12/702,636, entitled “Semiconductor Device And Semiconductor Assembly With Lead-Free Solder,” filed on Feb. 9, 2010. Both above-mentioned applications are incorporated herein by reference in its entirety.
This disclosure relates to the fabrication of integrated circuit devices, and more particularly, to the fabrication of bump structures in integrated circuit devices.
Modern integrated circuits are made 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.
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) layer located between the bump and an I/O pad. Recently, copper pillar bump technology has emerged. Instead of using solder bump, an electronic component is connected to a substrate by means of copper pillar bumps, which achieve finer pitches with minimum probability of bump bridging, reduces the capacitance load for the circuits, and allows the electronic component to perform at higher frequencies. It is within this context the following disclosure arises.
The present disclosure will be readily understood by the following detailed description in conjunction with the accompanying drawings, and like reference numerals designate like structural elements.
It is to be understood that the following disclosure provides many different embodiments, or examples, for implementing different features of the invention. Specific examples of components and arrangements are described below to simplify the present disclosure. These are, of course, merely examples and are not intended to be limiting. In addition, the present disclosure may repeat reference numerals and/or letters in the various examples. This repetition is for the purpose of simplicity and clarity and does not in itself dictate a relationship between the various embodiments and/or configurations discussed.
Substrate 101 may also include 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.
The material used for the conductive layer 105 may include, but not limited to, for example copper, aluminum, copper alloy, or other mobile conductive materials. If the conductive layer 105 is made of copper, there is a copper diffusion barrier layer (not shown) encasing the conductive layer 105 to prevent Cu from diffusing to device regions of substrate 101. The exemplary materials that can be used for copper diffusion barrier may include titanium, titanium nitride, tantalum, tantalum nitride, and combinations thereof.
The conductive layer 105 may be formed by electrochemical plating, electroless plating, sputtering, chemical vapor deposition (CVD), and the like. If a plating process is used to deposit conductive layer 105 made of copper, a copper seed layer (not shown) can be used to increase copper plating rate and quality. In some embodiments, the copper seed layer is deposited by sputtering or CVD process. The conductive layer 105 connects the metal interconnects underneath to bump features. The conductive layer 105 may a function as power lines, and re-distribution lines (RDL). Further, the conductive layer 105 may also function as inductors, capacitors or any passive components. Metal layer 105 may have a thickness less than about 30 μm, for example between about 2 μm and about 25 μm.
Next, a dielectric layer 109, also referred to as an isolation layer or a passivation layer, is formed on the substrate 101 and the conductive layer 105. The dielectric layer 109 may be formed of dielectric materials such as silicon nitride, silicon carbide, silicon oxynitride or other applicable materials. The formation methods include plasma enhance chemical vapor deposition (PECVD) or other commonly used CVD methods. In some embodiments, the dielectric layer 109 is optional. For example, if the conductive layer 105 is a PPI layer, the dielectric layer 109 is not needed, since a passivation layer is already deposited under the PPI layer. After the dielectric layer 109 is patterned, a polymer layer 110 is deposited. Following the deposition of the polymer layer 110, another lithographical process and another etching process are performed to pattern the polymer layer 110. As a result, an opening 120 is formed to pass through the polymer layer 110 and the dielectric layer 109 and expose a portion of the conductive layer 105 for allowing subsequent bump process. Although the sidewalls of layers 109 and 110 are drawn to be slanted in
The polymer layer 110, as the name suggests, is 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. In some embodiments, the polymer layer 110 is a polyimide layer. In some other embodiments, the polymer layer 110 is a polybenzoxazole (PBO) layer. The polymer layer 110 is soft, and hence has the function of reducing inherent stresses on respective substrate. In addition, the polymer layer 110 is easily formed to thickness of tens of microns.
Referring to
Next, a mask layer 122 is provided on the UBM layer 111 and patterned with an opening 123 exposing a portion of the UBM layer 111 for Cu pillar bump formation. In some embodiments, the opening 123 is over the opening 120. In some other embodiments, the diameter of the opening 123 is greater or equal to the diameter of the opening 120. In some embodiments, the size of the opening 123 is between about 5 μm to about 100 μm. The mask layer 112 may be a dry film or a photoresist film. The opening 123 is then partially or fully filled with a conductive material with solder wettability. In an embodiment, a metal layer 125 is formed in the opening 123 to contact the underlying UBM layer 111. The metal 125 protrudes above the surface of the polymer layer 110 with a thickness “D”. In some embodiments, the thickness “D” is between about 5 μm to about 100 μm. Other types of metal with high conductivity may also be used to fill opening 123, instead of Cu.
In some embodiments, the metal layer 125 is made of copper. As used throughout this disclosure, the term “copper (Cu) layer” is intended to include substantially a layer 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 metal layer 125. In some embodiments, the thickness of the Cu metal layer 125 is greater than 30 um. In some other embodiments, the thickness of the Cu metal layer is greater than 40 um. In some embodiments, the thickness of Cu metal layer 125 (thickness H as shown in
In some other embodiments, the metal layer 125 is made of solder. The solder metal layer 125 may be made of Sn, SnAg, Sn—Pb, SnAgCu (with Cu weight percentage less than 0.3%), SnAgZn, SnZn, SnBi—In, Sn—In, Sn—Au, SnPb, SnCu, SnZnIn, or SnAgSb, etc. 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 solder metal layer 125. In some embodiments, the thickness of the solder metal layer 125 is greater than 30 um. In some other embodiments, the thickness of the solder metal layer is greater than 40 um. In some embodiments, the thickness of solder metal layer 125 (thickness H as shown in
Afterwards, a cap layer 126 is formed on the top surface of the Cu metal layer 125, in accordance with some embodiments. The cap layer 126 could act as a barrier layer to prevent copper in the Cu pillar 125 from diffusing into a bonding material, such as solder alloy, that is used to bond the substrate 101 to external features. The prevention of copper diffusion increases the reliability and bonding strength of the package. The cap layer 126 may include nickel, tin, tin-lead (SnPb), gold (Au), silver, palladium (Pd), indium (In), nickel-palladium-gold (NiPdAu), nickel-gold (NiAu), other similar materials, or alloy. In some embodiments, the cap layer 126 is a nickel layer with a thickness about 1μ5 μm. In some embodiments, the cap layer 126 is formed by plating.
Afterwards, a solder layer 127 is formed on the cap layer 126, in accordance with some embodiments. The solder layer 127 may be lead-free or may contain lead. The solder layer 127 and the cap layer 126 may for a eutectic alloy, in some embodiments. The solder layer 127, the cap layer 126, and the Co pillar 125 are referred to as a bump structure 135 formed over the conductive layer 105. The solder layer 127 may be formed by plating. In some embodiments, the solder layer 127 is formed as solder ball on the cap layer 126. In some other embodiments, the solder layer 127 is a plated solder layer on the cap layer 126. For a lead-free solder system, the solder layer 127 is SnAg with Ag content being controlled lower than 1.6 weight percent (wt %), in accordance with some embodiments.
If the metal layer 125 is made of solder, the cap layer 126 and the lead-free solder layer 127 might not be needed. Further, if the metal layer 125 is made of solder, there may be additional layers between the UBM layer 111 and the metal layer 125. In some embodiments, a copper layer 131 and a diffusion barrier layer (a Ni layer) 132 are deposited on the UBM layer before the deposition of the solder metal layer 125′, as shown in
In some embodiments, the thickness of the copper layer 131 is between about 1 μm to about 10 μm. The thickness of the nickel layer 132 is between about 0.5 μm to about 5 μm. The copper layer 131 and the nickel layer 132 can be deposited by various methods, such as sputtering, chemical vapor deposition, and plating. The copper layer 131 and the nickel layer 132 in
Next, as shown in
If an isotropic wet etching is used to remove the exposed portion of the UBM layer 111, during the isotropic wet etching, a portion of the UBM layer 111 under Cu pillar bump 125 can be etched away (or undercut). As mentioned above, the UBM layer 111 can be formed of a diffusion barrier layer Ti layer (111L) and a seed layer Cu (layer 111U), as shown in
To ensure complete removal of exposed Cu layer (111U) and Ti layer (111L), overetching could be required. Overetching by wet etching chemistry(ies) leads to undercut, as shown in region A of
One way to resolve the Conductive-layer/adhesion-barrier-layer interfacial delamination issue is to improve the adhesion quality between the conductive Layer 105, which can be a metal-pad or a PPI, and the lower UBM layer 111L, which could an adhesion layer, such as Ti layer (111L). As shown in the exemplary process flow of making metal pillar bump involving
To improve the adhesion quality between conductive layer 105, such as the metal pad or PPI, and the UBM layer 111, such as a Ti layer 111L, a conductive protective layer that adheres well to both the conductive layer 105 and the lower UBM layer 111, can be deposited in-situ in the same system right after the deposition of the conductive layer 105.
The in-situ deposition (either in the same chamber or in separate chambers connected to a transfer chamber under vacuum) of the protective layer 108 over the conductive layer 105 prevents the conductive layer 105 from being exposed to oxygen to be oxidized. The conductive protective layer 108 is exposed to air and water during subsequent processing instead of the conductive layer 105. In some embodiments, the conductive protective layer 108 oxides at a rate relatively slower than the conductive layer 105. For example, Ti oxidizes at a slower rate than Al when exposed to air or water. In some other embodiments, the oxidized protective layer 108, such as titanium oxide, titanium oxynitride, tantalum oxide, tantalum oxynitride, etc., adheres better to the lower UBM layer 111L than the conductive layer 105. The strong bonding between the proactive layer 108 and the lower UBM layer 111L prevents interface delamination, which could have occurred under additional stress due to undercut of lower UBM layer 111L in region A of
The process flow for creating the structure shown in
As mentioned above, the lower UBM layer 111L may be formed of titanium, titanium nitride, tantalum, tantalum nitride, or a combination of above-mentioned materials. Since the protective layer 108 uses the same material as the lower UBM layer 111L, the lower UBM layer 111L can possibly be skipped to simplify the process flow. To skip the deposition of the lower UBM layer 111L, the upper UBM layer (Cu seed layer) needs to adhere well to the polymer layer 110. In addition, the concerns of copper diffusion from metal pillar bump 135 (or 135′) and/or copper seed layer 111U need to be resolved.
In some embodiments, the composite conductive layer is patterned and a dielectric material is used to fill the space between the patterned structures of the composite conductive layer. In some other embodiments, the composite conductive layer fills openings on the substrate and the composite conductive layer outside the openings are removed, such as by one or more chemical-mechanical planarization (CMP) processes. Afterward the formation of the composite conductive layer, a dielectric layer is deposited at operation 254. The dielectric layer has a thickness between about 500 Å to about 10,000 Å, in some embodiments. As mentioned above, the dielectric layer may also be referred to as an isolation layer or a passivation layer. Following operation 254, the dielectric layer is patterned and etched to create (or define, or form) an opening in the dielectric layer to expose the composite dielectric layer underneath at operation 255.
Afterwards, a polymer layer is deposited at operation 256, in accordance with some embodiments. The polymer layer is a relatively soft, often organic, dielectric material, and can be made of a material, such as an epoxy, polyimide, benzocyclobutene (BCB), polybenzoxazole (PBO), and the like. As described above, the polymer layer should adhere well with Cu. In some embodiments, the polymer material is made of poly(4,4′-oxydiphthalic anhydride-1,3-aminophenoxybenzene-8-azaadenine) (ODPA-APB-8-azaadenine). The polymer later has a thickness between about 500 Å to about 10,000 Å, in some embodiments.
Following the deposition of the polymer layer, the substrate is patterned and etched to create (or define, or form) an opening(s) to expose the composite conductive layer at operation 257 in order to form Cu pillar bumps, in some embodiments. Both the polymer layer and the dielectric layer under the openings are etched through to expose the protective layer. After operation 257, a plasma surface treatment is performed at operation 258 on the substrate surface to treat the polymer surface to increase the reactivity of to-be-deposited Cu with the plasma-treated polymer surface. As mentioned above, a plasma containing oxygen, nitrogen, or a combination of both can be used.
After plasma surface treatment of the polymer layer, a copper seed layer (UBM layer 111U) is deposited at operation 259, in accordance with embodiments. The copper seed layer has a thickness between about 100 Å to about 10,000 Å, in some embodiments. The copper seed layer comes in direct contact with the protective layer and promotes the growth of copper pillar bumps, which are to be deposited at a later operation. The copper seed layer can be deposited by PVD, CVD (chemical vapor deposition), ALD (atomic layer deposition), or electroless deposition. After the deposition of the copper seed layer, the substrate is patterned to create (or define, or form) an opening for copper deposition at operation 260, in accordance with some embodiments. The photoresist can be dry or wet. In some embodiments, the opening patterned at operation 260 is over and larger than the openings created at operation 257, as shown in
At operation 261, a metal layer, such as Cu, is deposited in the openings created in operations 260 and 257. In some embodiments, the copper film is deposited by electrochemical plating (ECP) or electroless plating. Other deposition methods are also applicable. Following the deposition of the copper layer, a cap layer, such as Ni, or other materials mentioned above, is deposited at operation 262 in accordance with some embodiments. In some embodiments, the cap layer is deposited by ECP or electroless plating. A solder layer is deposited over the cap layer at operation 263 in accordance with some embodiments. As mentioned above, the solder layer may be lead-free or may contain lead.
Afterwards, the photoresist (formed at operation 260) is removed at operation 264. At next operation 265, the exposed copper seed layer (not covered by copper pillar) is etched (or removed). At the end of operation 265 a Cu pillar bump is formed and the Cu pillar bump comes in contact with the composite conductive layer. In some embodiments, a reflow operation 266 is performed after operation 265 to make the shape of the lead-free solder layer rounded on the corner(s), as shown in
As described in
In the exemplary embodiments shown in
The mechanism of forming a metal bump structure described above resolves the delamination issues between a conductive layer on a substrate and a metal bump connected to the conductive layer. The conductive layer can be a metal pad, a post passivation interconnect (PPI) layer, or a top metal layer. By performing an in-situ deposition of a protective conductive layer over the conductive layer (or base conductive layer), the under bump metallurgy (UBM) layer of the metal bump adheres better to the conductive layer and reduces the occurrence of interfacial delamination. In some embodiments, a copper diffusion barrier sub-layer in the UBM layer can be removed, since the protective conductive layer is also a copper diffusion barrier. In these embodiments, a polymer, such as a polyimide, that adheres well with copper is used. In addition, a surface plasma treatment could be needed to create a copper diffusion barrier layer on the surface of the polymer. In some other embodiments, the UBM layer is not needed if the metal bump is deposited by a non-plating process and the metal bump is not made of copper.
In one embodiment, a bump structure on a substrate is provided. The bump structure includes a composite conductive layer on the substrate, and the composite conductive layer includes a protective conductive layer over a base conductive layer. The protective conductive layer and the base conductive layer are deposited in a system to prevent the oxidation of the base conductive layer. The composite conductive layer is made of a material less likely to be oxidized in presence of air or water than a material for the base conductive layer. The bump structure also includes a dielectric layer over the composite conductive layer, and a polymer layer over the dielectric layer. The bump structure further includes a metal bump, and the metal bump fills a second opening of a photoresist layer. The second opening is formed above a first opening created in the polymer layer to make contact with the protective conductive layer of the composite conductive layer, and the metal bump forms a strong bonding with the protective conductive layer.
In another embodiment, a bump structure on a substrate is provided. The bump structure includes a composite conductive layer on the substrate, and the composite conductive layer includes a protective conductive layer over a base conductive layer. The protective conductive layer and the base conductive layer are deposited in a system to prevent the oxidation of the base conductive layer, and the composite conductive layer is made of a material less likely to be oxidized in presence of air or water than a material for the base conductive layer. The bump structure also includes a dielectric layer over the composite conductive layer and a polymer layer over the dielectric layer. The bump structure further includes a copper bump, wherein the copper bump fills a second opening of a photoresist layer, and the second opening is formed above a first opening created in the polymer layer to make contact with the protective conductive layer of the composite conductive layer. The copper bump includes an under bump metallurgy (UBM) layer lining a surface of the first opening and an interface between the polymer layer and the photoresist layer, and the UBM layer forms a strong bonding with the protective conductive layer.
In yet another embodiment, a method of preparing a bump structure on a substrate is provided. The method includes forming a composite conductive layer on the substrate, and the composite conductive layer includes a base conductive layer and a protective conductive layer. The protective conductive layer is deposited right after the base conductive layer without exposing the substrate to air or water. The method also includes depositing a dielectric layer over the composite conductive layer and depositing a polymer layer over the dielectric layer. The method further includes forming a first opening for a copper pillar bump by etching through the dielectric layer and the polymer layer, and depositing an under bump metallurgy (UBM) layer. The UBM layer includes a copper seed layer. In addition, the method includes forming a photoresist pattern on the substrate, and the photoresist has a second opening defined over the first opening. Further, the method includes depositing a metal pillar bump layer, wherein both the UBM layer and the metal pillar bump layer are part of the bump structure.
Various modifications, changes, and variations apparent to those of skill in the art may be made in the arrangement, operation, and details of the methods and systems disclosed. Although the foregoing invention has been described in some detail for purposes of clarity of understanding, it will be apparent that certain changes and modifications may be practiced within the scope of the appended claims. Accordingly, the present embodiments are to be considered as illustrative and not restrictive, and the invention is not to be limited to the details given herein, but may be modified within the scope and equivalents of the appended claims.
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 |
5466635 | Lynch et al. | Nov 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 |
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 |
6576493 | Hirano | Jun 2003 | B1 |
6578754 | Tung | Jun 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 |
20040007779 | Arbuthnot et al. | Jan 2004 | A1 |
20040157450 | Bojkov et al. | Aug 2004 | 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 |
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 |
20070080421 | Suh | Apr 2007 | A1 |
20070108606 | Watanabe | May 2007 | A1 |
20070222073 | Farooq et al. | Sep 2007 | A1 |
20070284684 | Naito et al. | Dec 2007 | A1 |
20070287279 | Daubenspeck et al. | Dec 2007 | A1 |
20080080113 | Lin et al. | Apr 2008 | 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 |
20110101527 | Cheng et al. | May 2011 | A1 |
20110156256 | Kang et al. | Jun 2011 | A1 |
20110186990 | Mawatari et al. | Aug 2011 | A1 |
20110227216 | Tseng et al. | Sep 2011 | A1 |
20110281432 | Farooq et al. | Nov 2011 | A1 |
20110291267 | Wang et al. | Dec 2011 | A1 |
20120126419 | Kripesh et al. | May 2012 | A1 |
Number | Date | Country |
---|---|---|
101651120 | Feb 2010 | CN |
2125621 | May 1990 | JP |
1993335313 | Dec 1993 | JP |
2000228420 | Aug 2000 | JP |
2004048012 | Dec 2004 | JP |
20020027946 | Apr 2002 | KR |
20080052169 | Jun 2008 | KR |
2004004003 | Jan 2004 | WO |
Entry |
---|
Notice of Allowance for corresponding Patent Application No. 10-2011-0011567 (English Translation Version and Korean Language Version). |
Korean Office Action for corresponding Application No. 10-2011-0011567, with an English Translation. |
Chinese Office Action for corresponding Application No. 201010569645.9 (Chinese Language). |
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. |
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). |
Office Action dated Jun. 5, 2013 from corresponding application No. CN 201010569645.9. |
Number | Date | Country | |
---|---|---|---|
20110101527 A1 | May 2011 | US |
Number | Date | Country | |
---|---|---|---|
61258393 | Nov 2009 | US |