Embodiments of the present disclosure relate to methods of forming conductive elements for semiconductor devices and, in addition, to semiconductor structures that include such conductive elements.
Integrated circuits (ICs), the key components in thousands of electronic systems, generally include interconnected networks of electrical components fabricated on a common foundation, or substrate. Conductive interconnects are used to electrically connect semiconductor devices, such as capacitors or transistors, or to define a specific IC, such as a computer memory or microprocessor. The quality of the conductive interconnects greatly affects overall manufacturability, performance, and lifetime of the IC. Thus, the material used to form the conductive interconnects is increasingly determining the limits in performance, density, and reliability of integrated circuits.
For example, electrical conductivity of interconnects is extremely significant to the operational speed of the integrated circuit (IC). Aluminum (Al) and alloys thereof have been widely used as interconnect materials in semiconductor devices based on their low resistivity and ready adhesion to interlayer dielectric materials, such as silicon dioxide (SiO2). Unfortunately, aluminum is susceptible to corrosion and offers poor resistance to electromigration, which increases the potential for open circuits from voids or short circuits.
In an attempt to improve the performance, reliability, and density of the conductive interconnects, alternative metals to aluminum and aluminum alloys are being explored. To improve conductivity in the wiring, it has been proposed that copper (Cu) and alloys thereof be used to form conductive interconnects. However, copper rapidly diffuses through many conventional dielectric materials to form undesired copper oxide compounds. In addition, copper does not adhere well to conventional dielectric materials or to itself.
Silver (Ag) has also been proposed as a substitute for aluminum-containing conductive interconnects and is becoming increasingly significant in use as an electrochemically active material in electrodes of programmable memory cells, such as those of conductive bridge random access memory (conductive bridge RAM) cells. Silver has an extremely low resistivity, but is difficult to deposit in narrow gaps (e.g., gaps having a dimension of 20 nm or less) due to limitations on currently available deposition techniques. While silver may be deposited by sputtering (physical) deposition techniques, these techniques are not suitable for filling narrow gaps with silver. Furthermore, interconnects have been difficult to form from silver due to adhesion issues and agglomeration at increased temperatures. Since silver is resistant to dry etch processes, conventional techniques for forming semiconductor conductive elements (e.g., interconnects and electrodes) are impractical for making such conductive elements from silver.
FIGS. 3B1 through 3D are partial cross-sectional views of a semiconductor structure and illustrate a method of forming the conductive bridge RAM cell shown in
Methods of forming conductive elements, such as interconnects and electrodes, are disclosed, as are semiconductor structures and memory devices that include such conductive elements. The conductive element is formed from a silver material, such as silver or a silver alloy. Since silver has low resistivity and alloys and mixtures with other materials, the resistivity of the conductive element may be less than or equal to that of a conductive element formed from copper. In addition, use of a silver alloy or silver mixture may substantially reduce or eliminate issues with agglomeration associated with silver during thermal processing acts conducted at a later stage of semiconductor processing including such conductive elements. Using silver, a silver alloy, or a silver mixture may also enable narrow openings, such as those having at least one dimension of less than about 20 nm, to be filled.
As used herein, the term “alloy” means and includes a homogeneous mixture or solid solution of a plurality of materials (e.g., metals or nonmetals), with atoms of one of the materials occupying interstitial positions between atoms of another one of the materials. By way of example and not limitation, an alloy may include a mixture of silver and a metal selected from platinum, aluminum, tin, copper, iridium, titanium, nickel, cobalt, ruthenium, and rhodium.
As used herein, the term “mixture” means and includes a material formed by mixing a plurality of metals or a metal and a nonmetal. By way of example and not limitation, a mixture may include a mixture of silver and a metal such as tungsten.
As used herein, the term “liner” means and includes any structure that overlies a surface of at least one material. By way of example and not limitation, a liner may include a layer of material disposed over another material.
As used herein, the term “adhesion material” means and includes a material selected to facilitate adhesion of a first material to a second material immediately adjacent the first material.
As used herein, the term “chalcogenide” means and includes a material, including a glass or crystalline material, that includes an element from Group VIA (also identifiable as Group 16) of the periodic table of elements. Group VIA elements, often referred to as “chalcogens,” include sulfur (S), selenium (Se), tellurium (Te), polonium (Po), and oxygen (O). Examples of chalcogenides include, but are not limited to, germanium selenide (GeSe), germanium sulfide (GeS), germanium telluride (GeTe), indium selenide (InSe), and antimony selenide (SbSe). While the exemplary chalcogenides have a stoichiometry of one atom of each element, the chalcogenide may have other stoichiometries.
As used herein, the terms “redistribute” and “redistributing” mean and include spreading or smearing a material across a surface and into a partially filled, lined or, previously unfilled opening (e.g., via, trench) in a structure to fill or substantially fill the opening with the material.
As used herein, the term “substrate” means and includes a base material or construction upon which additional materials are formed. The substrate may be a semiconductor substrate, a base semiconductor layer on a supporting structure, a metal electrode or a semiconductor substrate having one or more layers, structures, or regions formed thereon. The substrate may be a conventional silicon substrate or other bulk substrate comprising a layer of semiconductive material. As used herein, the term “bulk substrate” means and includes not only silicon wafers, but also silicon-on-insulator (“SOI”) substrates, such as silicon-on-sapphire (“SOS”) substrates and silicon-on-glass (“SOG”) substrates, epitaxial layers of silicon on a base semiconductor foundation, and other semiconductor or optoelectronic materials, such as silicon-germanium, germanium, gallium arsenide, gallium nitride, and indium phosphide. The substrate may be doped or undoped.
The following description provides specific details, such as material types and processing conditions in order to provide a thorough description of embodiments of the present disclosure. However, a person of ordinary skill in the art will understand that the embodiments of the present disclosure may be practiced without employing these specific details. Indeed, the embodiments of the present disclosure may be practiced in conjunction with conventional semiconductor fabrication techniques employed in the industry. In addition, the description provided below does not form a complete process flow for manufacturing a semiconductor device. The semiconductor structures described below do not necessarily form a complete semiconductor device. Only those process acts and structures necessary to understand the embodiments of the present disclosure are described in detail below. Additional acts to form a complete semiconductor device from the semiconductor structures may be performed by conventional fabrication techniques.
The semiconductor structure 100 may, optionally, include an electrode material 108 (shown in broken lines) between the material 104 and the substrate 102. The electrode material 108 may be formed from a conductive material, such as tungsten (W), platinum (Pt), titanium nitride (TiN), or nickel (Ni). The electrode material 108 may be formed over the substrate 102 using a conventional deposition process, such as a chemical vapor deposition process or an atomic layer deposition process. While
The opening 106 may be formed by removing a portion of the material 104 using, for example, conventional photolithography techniques (e.g., masking and etching) known in the art of integrated circuit fabrication. By way of non-limiting example, the opening 106 may extend longitudinally into a plane of
Referring to
Referring to
The thicknesses of the liner material 110 and the conductive material 112 may be selected based on a desired ratio of materials. In embodiments in which the liner material 110 includes platinum and the conductive material 112 includes silver, a ratio of the liner material 110 to the conductive material 112 may be less than or equal to about 1 to 2.
Referring to
In embodiments in which the liner material 110 is formed from a material that does not form an alloy with the conductive material 112, the annealing process may be bypassed and the liner material 110 may remain at the interface between the conductive material 112 and the material 104 and, if present, the electrode material 108 (as shown in
An exposed surface of the semiconductor structure 100 may be subjected to a material removal process, such as a so-called polishing process in the form of, for example, a chemical mechanical polishing (CMP) process or a mechanical polishing process, to form an interconnect 120, as shown in
The polishing process may be a chemical mechanical polishing process that is performed using a conventional chemical mechanical polishing apparatus and a slurry that enables redistribution of the malleable materials (e.g., the conductive material 112 and, optionally, the liner material 110) into the unfilled region 116 of the opening 106 to form the interconnect 120. Such a slurry may be, for example, an alumina-based slurry at a neutral or slightly basic pH that is substantially free of oxidizer. The polishing process may also be a mechanical polishing process performed using the conventional chemical mechanical polishing apparatus and water (e.g., deionized water) instead of a chemical slurry. Using water as the liquid component in the polishing process, without addition of chemical etching agents, may enable redistribution of the conductive material 112 and the liner material 110, if present, into the unfilled region of the opening 106 without substantially removing such materials.
After forming the interconnect 120, another annealing process may, optionally, be performed. By way of example and not limitation, this annealing process may include exposing the semiconductor structure 100 of
For the sake of simplicity, the methods described with respect to
Referring to
Referring to
The thicknesses of the liner material 210 and the conductive material 212 may be selected based on a desired ratio of materials. In embodiments in which the liner material 210 includes platinum and the conductive material 212 includes silver, a ratio of the liner material 210 to the conductive material 212 may be less than or equal to about 1 to 2.
Referring to
In embodiments in which the liner material 210 is formed from a material that does not form an alloy with the conductive material 212, the annealing process may be bypassed and the liner material 210 may remain over the conductive material 212 (as shown in
An exposed surface of the semiconductor structure 200 may be subjected to a material removal process, such as a so-called polishing process in the form of a chemical mechanical polishing (CMP) process or a mechanical polishing process, to form an interconnect 220, as shown in
After forming the interconnect 220, another annealing process may, optionally, be performed. By way of example and not limitation, the annealing process may include exposing the semiconductor structure 200 to a temperature of between about 100° C. and about 500° C. and, more particularly, to a temperature of about 200° C. The annealing process may result in formation of an alloy of the conductive material 212 and the liner material 210, as previously discussed. After annealing, the interconnect 220 may include regions of the conductive material 212, the liner material 210, and the alloy or may substantially include the alloy.
For the sake of simplicity, the methods described with respect to
While not wishing to be bound by any particular theory, it is believed that operation of the conductive bridge RAM cell 330 occurs due to selective formation and dissolution of a conductive bridge formed by electromigration of silver into the memory material 309. Thus, it is important to control diffusion of silver ions into the memory material 309 during deposition of the second electrode 311.
FIGS. 3B1 through 3D illustrate embodiments of a method of forming the conductive bridge RAM cell 330 shown in
The interlayer dielectric material 305 may be formed from, for example, silicon nitride, silicon dioxide, or a silicon oxynitride. The interlayer dielectric material 305 may be formed over the first electrode 308 using a conventional deposition process, such as a chemical vapor deposition process, an atomic layer deposition process, or a physical vapor deposition process.
The conductive structure 303 may be formed from a conductive material, such as at least one of titanium nitride, tungsten, tungsten nitride, tantalum, and tantalum nitride. The conductive structure 303 may be formed in electrical connection with the first electrode 308. The conductive structure 303 may be formed in the interlayer dielectric material 305 using conventional techniques, the details of which are known in the art and, therefore, are not described in detail herein. For example, a conventional damascene process may be used to form the conductive structure 303 in the interlayer dielectric material 305 by forming a trench in the interlayer dielectric material 305, forming the conductive material over interlayer dielectric material 305 to fill the trench, and performing a chemical mechanical polishing (CMP) process to remove portions of the conductive material overlying the interlayer dielectric material 305.
The memory material 309 may be formed from a chalcogenide material, such as germanium selenide or germanium sulfide, or an oxide material, such as a high-k oxide material. Examples of suitable high-k dielectric materials include, but are not limited to, silicon dioxide, tantalum oxide, titanium oxide, nitrogen oxide, zirconium oxide, and hafnium oxide. For example, the memory material 309 may be deposited using a conventional deposition process, such as a physical vapor deposition process, a chemical vapor deposition process, or an atomic layer deposition process.
The dielectric material 304 may be formed from, for example, silicon nitride, tetraethyl orthosilicate (TEOS), silicon dioxide, or a silicon oxynitride. The dielectric material 304 may be formed over the interlayer dielectric material 305 and the conductive structure 303 using a conventional deposition process, such as a chemical vapor deposition process, an atomic layer deposition process, or a physical vapor deposition process. In some embodiments, the dielectric material 304 may be formed as a monolithic structure. In other embodiments, the dielectric material 304 may be formed as a stacked structure that includes a plurality of materials 304A, 304B, 304C, as shown in broken lines. For example, the materials 304A and 304C may be formed from silicon nitride and the material 304B may be formed from tetraethyl orthosilicate.
The opening 306 may be formed in the dielectric material 304 by removing a portion of the dielectric material 304 using, for example, conventional photolithography techniques (e.g., masking and etching) known in the art of integrated circuit fabrication. The portion of the dielectric material 304 removed to form the opening 306 may overlie the conductive structure 303 such that the opening 306 exposes a surface of the conductive structure 303 and, optionally, surfaces of the interlayer dielectric material 305 adjacent the surface of the conductive structure 303. By way of example and not limitation, the opening 306 may have a width W3 of less than about 100 nm and, more particularly, less than about 20 nm.
Referring to FIG. 3B2, the memory material 309 may alternatively be formed over sidewalls of the dielectric material 304 and surfaces of the conductive structure 303 and the interlayer dielectric material 305 after forming the dielectric material 304 and the opening 306 in the dielectric material 304. As previously discussed with respect to FIG. 3B1, the memory material 309 may be formed from a chalcogenide material, such as germanium selenide or germanium sulfide, or an oxide material, such as a high-k oxide material, using a conventional deposition process, such as a physical vapor deposition process, a chemical vapor deposition process, or an atomic layer deposition process.
After deposition of the memory material 309, an annealing process may optionally be performed. By way of example and not limitation, the annealing process may include exposing the semiconductor structure 300 to a temperature of between about 100° C. and about 500° C. and, more particularly, a temperature of about 200° C.
As shown in
Forming silver using a conventional vapor deposition process, such as a physical vapor deposition (PVD) process or a chemical vapor deposition (CVD) process, may cause undesirable diffusion of the silver into the memory material 309 during formation of the second electrode 311 (
Referring to
Removal of silver from unwanted areas may be complicated as there are currently no known etchants for selectively removing the silver with respect to the other materials. Thus, material (i.e., the conductive material 312 and the liner material 310) may be pushed or redistributed from upper surfaces of the dielectric material 304 into voids (e.g., the unfilled region 316 of the opening 306 (
In
A plurality of trenches was formed in a silicon dioxide material overlying a silicon wafer. The trenches of the plurality each had a depth of about 50 nm. Silver was deposited over the surface of the silicon wafer using a conventional sputtering process. The sputtering process was performed using a conventional sputter coater. The silver was sputtered over the surface of the silicon wafer for about two minutes, during which time the silver reached a thickness of about 15 nm. Platinum was then formed over the silver using the sputter coater. The platinum was sputtered over the surface of the silicon wafer for about 30 seconds, during which time the platinum reached a thickness of about 6 nm.
A mechanical polishing process was performed on the silicon wafer having the silver and platinum thereon using deionized water and a conventional polishing pad. No chemical slurry was used during the mechanical polishing process. The surface of the platinum was polished using a pad rotation of about 100 RPM. After the mechanical polishing process, a scanning electron microscope (SEM) was used to observe that the trenches were substantially filled with material (e.g., the silver and the platinum).
An annealing process was then performed using a conventional industrial oven. The industrial oven was set to 200° C., and the silicon wafer having the silver and platinum thereon was placed therein for about 10 minutes. It was confirmed that the post-annealed silver-platinum alloy was substantially smooth with low resistance.
In one embodiment, the present disclosure includes methods of forming at least one conductive element. Such a method may include forming a first conductive material over a structure comprising at least one opening defined by sidewalls of a dielectric material, forming a second conductive material comprising silver over the first conductive material, and annealing the structure to form a material comprising at least a portion of the first conductive material and the second conductive material.
A method of forming the conductive element may also include forming a conductive material comprising silver over surfaces of a structure comprising at least one opening defined by sidewalls of a dielectric material, forming another conductive material over the conductive material, and performing a polishing process to substantially redistribute at least one of the conductive material and the another conductive material into an unfilled region of the at least one opening.
In a further embodiment, the present disclosure includes a method of forming a semiconductor structure. The method may include removing a portion of a dielectric material overlying a substrate to form at least one opening therein, forming a first conductive material over the dielectric material and exposed surfaces of the at least one opening, forming a second conductive material comprising silver over the first conductive material, a portion of the at least one opening remaining unfilled, and performing a polishing process to substantially fill the unfilled portion of the at least one opening.
In yet another embodiment, the present disclosure includes a method of forming a memory cell. The method includes forming a first conductive material over surfaces of a structure comprising at least one opening overlying a first electrode, forming a memory material over the first conductive material, forming a second conductive material comprising silver over the memory material, a portion of the at least one opening remaining unfilled, and performing a process to substantially fill the at least one opening with the memory material and the second conductive material.
The method of forming the memory cell may also include forming a first conductive material comprising silver over surfaces of a memory material exposed by at least one opening overlying a first electrode, forming a second conductive material over the first conductive material, a portion of the at least one opening remaining unfilled, and performing a process to substantially fill the at least one opening with the memory material and the first and second conductive materials.
In yet another embodiment, the present disclosure includes a semiconductor structure. The semiconductor structure may include a conductive structure overlying an electrode, at least one of a chalcogenide material and an oxide material in contact with the conductive structure, and a conductive material overlying the chalcogenide material, the conductive material comprising silver, and at least one region comprising another material.
In further embodiments, the present disclosure includes a memory cell. The memory cell includes a memory material overlying an electrode. The memory cell also includes a conductive material comprising silver and another material. The conductive material overlies the memory material and is disposed in at least one opening.
While the invention is susceptible to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and have been described in detail herein. However, the invention is not intended to be limited to the particular forms disclosed. Rather, the invention is to cover all modifications, equivalents, and alternatives falling within the scope of the invention as defined by the following appended claims and their legal equivalents.
This application is a continuation of U.S. patent application Ser. No. 15/848,399, filed Dec. 20, 2017, now U.S. Pat. No. 10,411,186, issued Sep. 10, 2019, which is a continuation of U.S. patent application Ser. No. 15/375,457, filed Dec. 12, 2016, now U.S. Pat. No. 9,865,812, issued Jan. 9, 2018, which is a divisional of U.S. patent application Ser. No. 13/961,479, filed Aug. 7, 2013, now U.S. Pat. No. 9,520,558, issued Dec. 13, 2016, which is a divisional of U.S. patent application Ser. No. 13/050,725, filed Mar. 17, 2011, now U.S. Pat. No. 8,524,599, issued Sep. 3, 2013, the disclosure of each of which is hereby incorporated herein in its entirety by this reference.
Number | Name | Date | Kind |
---|---|---|---|
5529954 | Iijima et al. | Jun 1996 | A |
5719447 | Gardner | Feb 1998 | A |
6100194 | Chan et al. | Aug 2000 | A |
6143655 | Forbes et al. | Nov 2000 | A |
6465345 | Nogami et al. | Oct 2002 | B1 |
6511906 | Sinha | Jan 2003 | B1 |
6709971 | Kozhukh et al. | Mar 2004 | B2 |
6757971 | Sinha | Jul 2004 | B2 |
6936545 | Xie et al. | Aug 2005 | B1 |
6946392 | Sinha | Sep 2005 | B2 |
6969301 | Sinha | Nov 2005 | B2 |
7033930 | Kozhukh et al. | Apr 2006 | B2 |
7118707 | Robinson | Oct 2006 | B2 |
7199052 | Cohen | Apr 2007 | B2 |
7229924 | Farrar | Jun 2007 | B2 |
7332401 | Moore et al. | Feb 2008 | B2 |
7423282 | Park et al. | Sep 2008 | B2 |
7694871 | Ronay | Apr 2010 | B2 |
7718537 | Ufert | May 2010 | B2 |
8524599 | Tang et al. | Sep 2013 | B2 |
9520558 | Tang et al. | Dec 2016 | B2 |
20030041452 | Sinha | Mar 2003 | A1 |
20030047771 | Kweon et al. | Mar 2003 | A1 |
20030134436 | Yates et al. | Jul 2003 | A1 |
20030143838 | Kozhukh et al. | Jul 2003 | A1 |
20030203526 | Lin et al. | Oct 2003 | A1 |
20040038523 | Kozhukh et al. | Feb 2004 | A1 |
20040155349 | Nakamura et al. | Aug 2004 | A1 |
20050282378 | Fukunaga et al. | Dec 2005 | A1 |
20060046453 | Collins et al. | Mar 2006 | A1 |
20060084271 | Yang et al. | Apr 2006 | A1 |
20060094236 | Elkins et al. | May 2006 | A1 |
20060289999 | Lee et al. | Dec 2006 | A1 |
20070018329 | Oh et al. | Jan 2007 | A1 |
20070139987 | Kouchiyama et al. | Jun 2007 | A1 |
20070145586 | Onishi et al. | Jun 2007 | A1 |
20080036508 | Sakamoto et al. | Feb 2008 | A1 |
20080128912 | Streck et al. | Jun 2008 | A1 |
20080253165 | Blanchard | Oct 2008 | A1 |
20090239398 | Lynch et al. | Sep 2009 | A1 |
20100003814 | Lee et al. | Jan 2010 | A1 |
20100078820 | Kurokawa et al. | Apr 2010 | A1 |
20100163829 | Wang et al. | Jul 2010 | A1 |
20100193758 | Tian et al. | Aug 2010 | A1 |
20100197132 | Ahn et al. | Aug 2010 | A1 |
20110115096 | Bradl et al. | May 2011 | A1 |
20120235106 | Tang et al. | Sep 2012 | A1 |
20130320291 | Tang et al. | Dec 2013 | A1 |
Number | Date | Country |
---|---|---|
1822327 | Aug 2006 | CN |
100533674 | Aug 2009 | CN |
2000-040742 | Feb 2000 | JP |
2003-133534 | May 2003 | JP |
2004-235620 | Aug 2004 | JP |
2007-027769 | Feb 2007 | JP |
2007-157941 | Jun 2007 | JP |
2007-157942 | Jun 2007 | JP |
2007-180173 | Jul 2007 | JP |
591705 | Jun 2004 | TW |
Entry |
---|
First Office Action Issued by State Intellectual Property Office and Search Report for Chinese Application No. 2012800188611, (action dated Dec. 3, 2014) (search report dated Nov. 17, 2014), 8 pages (including English translation). |
Gao et al., Thermal Stability of Titanium Nitride Diffusion Barrier Films for Advanced Silver Interconnects, Microelectronic Engineering, vol. 76, 2004, pp. 76-81. |
International Preliminary Report on Patentability for PCT Application No. PCT/US2012/028878, (dated Sep. 17, 2013), 6 pages. |
Korean Office Action for Korean Application No. 10-2013-7025995 dated Sep. 25, 2014, 4 pages. |
Korean Office Action for Korean Application No. 10-2013-7025995 dated Sep. 5, 2014, 10 pages. |
Korean Written Opinion for Korean Application No. 10-2013-7025995 dated Sep. 5, 2014, 4 pages. |
Korean Written Opinion for Korean Application No. 10-2013-7025995, dated Jun. 2, 2014, 8 pages. |
Notice of Reasons for Refusal for Japanese Application No. 2014-135499, (dated Apr. 21, 2015), 10 pages (including English translation of sections indicated by annotation). |
Notification of Reexamination for Chinese Application No. 201280018861.1, (dated Aug. 25, 2016), 11 pages (including English translation). |
Office Action (Communication pursuant to Article 94(3) EPC) for European Application No. 12757934.0, (dated Jun. 12, 2015), 4 pages. |
Office Action (Communication) and Supplementary European Search Report for European Application No. 12757934.0, (search completed Jul. 24, 2014) (dated Aug. 4, 2014), 9 pages. |
Office Action and Search Report for Taiwanese Application No. 101109223, (search completed Jan. 14, 2014) (action dated Jan. 15, 2014), 7 pages (including English translation). |
Office Action and Search Report for Taiwanese Application No. 103120618, (search completed Dec. 7, 2015) (action dated Dec. 14, 2015), 10 pages (including English translation). |
PCT International Search Report and Written Opinion for PCT Application No. PCT/US2012/028878, dated Oct. 16, 2012. |
Rejection Decision for Chinese Application No. 201280018861.1, (dated Feb. 2, 2016), 15 pages (including English translation). |
Second Office Action Issued by State Intellectual Property Office for Chinese Application No. 201280018861.1, (dated Jul. 1, 2015), 13 pages (including English translation). |
Ushiku Y. et al., Planarized silver interconnect technology with a Ti self-p. assivation technique for deep sub-micron ULSis, VLSI technology 1993 digest of technical papers, 1993, pp. 121-122. |
Chinese Office Action from Chinese Application No. 201710243903.6, dated Feb. 3, 2020, 20 pages. |
Number | Date | Country | |
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20190363253 A1 | Nov 2019 | US |
Number | Date | Country | |
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Parent | 13961479 | Aug 2013 | US |
Child | 15375457 | US | |
Parent | 13050725 | Mar 2011 | US |
Child | 13961479 | US |
Number | Date | Country | |
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Parent | 15848399 | Dec 2017 | US |
Child | 16538477 | US | |
Parent | 15375457 | Dec 2016 | US |
Child | 15848399 | US |