High purity aluminum top coat on substrate

Information

  • Patent Grant
  • 10774436
  • Patent Number
    10,774,436
  • Date Filed
    Monday, November 13, 2017
    6 years ago
  • Date Issued
    Tuesday, September 15, 2020
    3 years ago
Abstract
A chamber component for a processing chamber comprises an article having impurities, an aluminum coating on a surface of the article, wherein the aluminum coating is substantially free from impurities, and an anodization layer over the aluminum coating. The anodization layer comprises aluminum oxide. The anodization layer further comprises a dense barrier layer portion and a porous columnar layer portion.
Description
TECHNICAL FIELD

Embodiments of the present disclosure relate, in general, to aluminum coated articles and to a process for applying an aluminum coating to a substrate.


BACKGROUND

In the semiconductor industry, devices are fabricated by a number of manufacturing processes producing structures of an ever-decreasing size. Some manufacturing processes may generate particles, which frequently contaminate the substrate that is being processed, contributing to device defects. As device geometries shrink, susceptibility to defects increases, and particle contaminant requirements become more stringent. Accordingly, as device geometries shrink, allowable levels of particle contamination may be reduced.


SUMMARY

In one embodiment, an aluminum coating is formed on an article, and the aluminum coating is anodized to form an anodization layer. The anodization layer can have a thickness in a range between 40% to 60% of the thickness of the aluminum coating. The anodization layer can also have a thickness up to 2 to 3 times the thickness of the aluminum coating.


In one embodiment, the aluminum is a high purity aluminum. The aluminum coating may have a thickness in a range from about 0.8 mils to about 4 mils. The anodization layer may have a thickness in a range from about 0.4 to about 4 microns. In one embodiment, a surface roughness of the anodization layer is about 40 micro-inch.


In one embodiment, the article can include at least one of aluminum, copper, magnesium, an aluminum alloy (e.g., Al6061), or a ceramic material.


In one embodiment, the aluminum coating is formed by electroplating. About half of the anodization layer can be formed from conversion of the aluminum coating during anodization.





BRIEF DESCRIPTION OF THE DRAWINGS

The present disclosure is illustrated by way of example, and not by way of limitation, in the figures of the accompanying drawings in which like references indicate similar elements. It should be noted that different references to “an” or “one” embodiment in this disclosure are not necessarily to the same embodiment, and such references mean at least one.



FIG. 1 illustrates an exemplary architecture of a manufacturing system, in accordance with one embodiment of the present invention.



FIG. 2 illustrates a process for electroplating a conductive article with aluminum, in accordance with one embodiment of the present invention.



FIG. 3 illustrates a process for anodizing an aluminum coated conductive article, in accordance with one embodiment of the present invention.



FIG. 4 illustrates a process for manufacturing an aluminum coated conductive article, in accordance with one embodiment of the present invention.



FIG. 5 illustrates a cross-sectional view of one embodiment of an aluminum coating on a conductive article.



FIG. 6 illustrates a cross-sectional view of one embodiment of an aluminum coating and an anodization layer on a conductive article.





DETAILED DESCRIPTION OF EMBODIMENTS

Embodiments of the disclosure are directed to a process for coating an article (e.g., for use in semiconductor manufacturing) with an aluminum coating, and to an article created using such a coating process. In one embodiment, the article is coated, and then at least a portion of the coating is anodized. For example, the article may be a showerhead, a cathode sleeve, a sleeve liner door, a cathode base, a chamber liner, an electrostatic chuck base, etc. of a chamber for processing equipment such as an etcher, a cleaner, a furnace, and so forth. In one embodiment, the chamber is for a plasma etcher or plasma cleaner. In one embodiment, these articles can be formed of an aluminum alloy (e.g., Al 6061), another alloy, a metal, a metal oxide, a ceramic, or any other suitable material. The article may be a conductive article (e.g., an aluminum alloy) or a non-conductive or insulating article (e.g., a ceramic).


Parameters for the anodization may be optimized to reduce particle contamination from the article. Performance properties of the aluminum coated article may include a relatively long lifespan, and a low on-wafer particle and metal contamination.


Embodiments described herein with reference to aluminum coated conductive articles may cause reduced particle contamination and on wafer metal contamination when used in a process chamber for plasma rich processes. However, it should be understood that the aluminum coated articles discussed herein may also provide reduced particle contamination when used in process chambers for other processes such as non-plasma etchers, non-plasma cleaners, chemical vapor deposition (CVD) chamber, physical vapor deposition (PVD) chamber, and so forth.


When the terms “about” and “approximately” are used herein, these are intended to mean that the nominal value presented is precise within ±10%. The articles described herein may be other structures that are exposed to plasma.



FIG. 1 illustrates an exemplary architecture of a manufacturing system 100. The manufacturing system 100 may be a system for manufacturing an article for use in semiconductor manufacturing. In one embodiment, the manufacturing system 100 includes processing equipment 101 connected to an equipment automation layer 115. The processing equipment 101 may include one or more wet cleaners 103, an aluminum coater 104 and/or an anodizer 105. The manufacturing system 100 may further include one or more computing device 120 connected to the equipment automation layer 115. In alternative embodiments, the manufacturing system 100 may include more or fewer components. For example, the manufacturing system 100 may include manually operated (e.g., off-line) processing equipment 101 without the equipment automation layer 115 or the computing device 120.


Wet cleaners 103 are cleaning apparatuses that clean articles (e.g., conductive articles) using a wet clean process. Wet cleaners 103 include wet baths filled with liquids, in which the substrate is immersed to clean the substrate. Wet cleaners 103 may agitate the wet bath using ultrasonic waves during cleaning to improve a cleaning efficacy. This is referred to herein as sonicating the wet bath.


In one embodiment, wet cleaners 103 include a first wet cleaner that cleans the articles using a bath of de-ionized (DI) water and a second wet cleaner that cleans the articles using a bath of acetone. Both wet cleaners 103 may sonicate the baths during cleaning processes. The wet cleaners 103 may clean the article at multiple stages during processing. For example, wet cleaners 103 may clean an article after a substrate has been roughened, after an aluminum coating has been applied to the substrate, after the article has been used in processing, and so forth.


In other embodiments, alternative types of cleaners such as dry cleaners may be used to clean the articles. Dry cleaners may clean articles by applying heat, by applying gas, by applying plasma, and so forth.


Aluminum coater 104 is a system configured to apply an aluminum coating to the surface of the article. In one embodiment, aluminum coater 104 is an electroplating system that plates the aluminum on the article (e.g., a conductive article) by applying an electrical current to the article when the article is immersed in an electroplating bath including aluminum, which will be described in more detail below. Here, surfaces of the article can be coated evenly because the conductive article is immersed in the bath. In alternative embodiments, the aluminum coater 104 may use other techniques to apply the aluminum coating such as physical vapor deposition (PVD), chemical vapor deposition (CVD), twin wire arc spray, ion vapor deposition, sputtering, and cold spray.


In one embodiment, anodizer 105 is a system configured to form an anodization layer on the aluminum coating. For example, the article (e.g., a conductive article) is immersed in an anodization bath, e.g., including sulfuric acid or oxalic acid, and an electrical current is applied to the article such that the article is an anode. The anodization layer then forms on the aluminum coating on the article, which will be discussed in more detail below.


The equipment automation layer 115 may interconnect some or all of the manufacturing machines 101 with computing devices 120, with other manufacturing machines, with metrology tools and/or other devices. The equipment automation layer 115 may include a network (e.g., a location area network (LAN)), routers, gateways, servers, data stores, and so on. Manufacturing machines 101 may connect to the equipment automation layer 115 via a SEMI Equipment Communications Standard/Generic Equipment Model (SECS/GEM) interface, via an Ethernet interface, and/or via other interfaces. In one embodiment, the equipment automation layer 115 enables process data (e.g., data collected by manufacturing machines 101 during a process run) to be stored in a data store (not shown). In an alternative embodiment, the computing device 120 connects directly to one or more of the manufacturing machines 101.


In one embodiment, some or all manufacturing machines 101 include a programmable controller that can load, store and execute process recipes. The programmable controller may control temperature settings, gas and/or vacuum settings, time settings, etc. of manufacturing machines 101. The programmable controller may include a main memory (e.g., read-only memory (ROM), flash memory, dynamic random access memory (DRAM), static random access memory (SRAM), etc.), and/or a secondary memory (e.g., a data storage device such as a disk drive). The main memory and/or secondary memory may store instructions for performing heat treatment processes described herein.


The programmable controller may also include a processing device coupled to the main memory and/or secondary memory (e.g., via a bus) to execute the instructions. The processing device may be a general-purpose processing device such as a microprocessor, central processing unit, or the like. The processing device may also be a special-purpose processing device such as an application specific integrated circuit (ASIC), a field programmable gate array (FPGA), a digital signal processor (DSP), network processor, or the like. In one embodiment, programmable controller is a programmable logic controller (PLC).



FIG. 2 illustrates a process for electroplating an article (e.g., a conductive article) with aluminum, in accordance with one embodiment of the present invention. Electroplating may produce an aluminum layer having a purity of 99.99. Electroplating is a process that uses electrical current to reduce dissolved metal cations to form a metal coating on an electrode, e.g., article 203. The article 203 is the cathode, and an aluminum body 205 (e.g., high purity aluminum) is the anode. Both components are immersed in an aluminum plating bath 201 including an electrolyte solution containing one or more dissolved metal salts as well as other ions that permit the flow of electricity. A current supplier 207 (e.g., a battery or other power supply) supplies a direct current to the article 203, oxidizing the metal atoms of the aluminum body 205 such that the metal atoms dissolve in the solution. The dissolved metal ions in the electrolyte solution are reduced at the interface between the solution and the article 203 to plate onto the article 203 and form an aluminum plating layer. The aluminum plating is typically smooth. For example, the aluminum plating may have a surface roughness (Ra) of about 20 micro-inch to about 200 micro-inch.


In one embodiment, the aluminum plating layer thickness is optimized for both cost savings and adequate thickness for anodization. Half of thickness of the anodization layer may be based on consumption of the thickness of the aluminum plating layer. In one embodiment, the anodization layer consumes all of the aluminum layer. Thus, the thickness of the aluminum layer may be half of the target thickness of the anodization layer. In another embodiment, the aluminum plating layer may be formed to have a thickness that is twice that of the desired thickness of the anodization layer. Other thicknesses of the aluminum plating layer may also be used. In one embodiment, the aluminum plating layer has a thickness of 5 mils. In one embodiment, the aluminum plating layer has a thickness in a range from about 0.8 mils to about 4 mils. Note that other aluminum coating processes other than electroplating may also be used in other embodiments.



FIG. 3 illustrates a process for anodizing an aluminum coated article 303, according to one embodiment. Note that in some embodiments anodization is not performed. For example, the article 303 can be the article 203 of FIG. 2. Anodization changes the microscopic texture of the surface of the article 303. Preceding the anodization process, the article 303 can be cleaned in a nitric acid bath or brightened in a mix of acids, i.e., be subjected to a chemical treatment (e.g., deoxidation) prior to anodization.


The article 303 is immersed in an anodization bath 301, including an acid solution, along with a cathode body 305. Examples of cathode bodies that may be used include aluminum alloys such as Al6061 and Al3003 and carbon bodies. The anodization layer is grown on the article 303 by passing a current through an electrolytic solution via a current supplier 307 (e.g., a battery or other power supply), where the article is the anode (the positive electrode). The current releases hydrogen at the cathode body, e.g., the negative electrode, and oxygen at the surface of the article 303 to form aluminum oxide. In one embodiment, the voltage that enables anodization using various solutions may range from 1 to 300 V, in one embodiment, or from 15 to 21 V, in another embodiment. The anodizing current varies with the area of the aluminum body 305 anodized, and can range from 30 to 300 amperes/meter2 (2.8 to 28 ampere/ft2).


The acid solution dissolves (i.e., consumes or converts) a surface of the article (e.g., the aluminum coating) to form a coating of columnar nanopores, and the anodization layer continues growing from this coating of nanopores. The columnar nanopores may be 10 to 150 nm in diameter. The acid solution can be oxalic acid, sulfuric acid, or a combination of oxalic acid and sulfuric acid. For oxalic acid, the ratio of consumption of the article to anodization layer growth is about 1:1. For sulfuric acid, the ratio of consumption of the article to anodization layer growth is about 2:1. Electrolyte concentration, acidity, solution temperature, and current are controlled to form a consistent aluminum oxide anodization layer. In one embodiment, the anodization layer can have a thickness of up to 4 mils. In one embodiment, the anodization layer has a minimum thickness of 0.4 mils. In one embodiment, the anodization layer has a thickness in a range between 40% to 60% of the thickness of the aluminum coating. In one embodiment, the anodization layer has a thickness in a range between 30% to 70% of the thickness of the aluminum coating, though the anodization layer can have thicknesses that are other percentages of the aluminum coating. In one embodiment, all of the aluminum layer is anodized. Accordingly, the anodization layer may have a thickness that is twice the thickness of the aluminum coating (for anodization performed using oxalic acid) or that is approximately 1.5 times the thickness of the aluminum coating (for anodization performed using sulfuric acid).


In one example, if oxalic acid is used to perform the anodization, the aluminum coating is initially 4 mils thick, the resulting anodization layer may be 4 mils thick, and a resulting aluminum coating after the anodization may be 2 mils thick. In another example, if sulfuric acid is used to perform the anodization, the aluminum coating is initially 4 mils thick, the resulting anodization layer may be 3 mils thick, and a resulting aluminum coating after the anodization may be 2 mils thick. In one embodiment, a thicker aluminum coating is used if sulfuric acid is to be used for the anodization.


In one embodiment, the current density is initially high to grow a very dense barrier layer portion of the anodization layer, and then current density is reduced to grow a porous columnar layer portion of the anodization layer. In one embodiment where oxalic acid is used to form the anodization layer, the porosity is in a range from about 40% to about 50%, and the pores have a diameter in a range from about 20 nm to about 30 nm. In one embodiment where sulfuric acid is used to form the anodization layer, the porosity can be up to about 70%.


In one embodiment, the surface roughness (Ra) of the anodization layer is about 40 micro-inch, which is similar to the roughness of the article. In one embodiment, the surface roughness increases 20-30% after anodizing with sulfuric acid.


In one embodiment, the aluminum coating is about 100% anodized. In one embodiment, the aluminum coating is not anodized.


Table A shows the results of laser ablation inductively coupled plasma mass spectrometry (ICPMS) used to detect metallic impurities in an Al6061 article, an anodized Al6061 article, an aluminum coating including an aluminum plating layer on an Al6061 article, and an anodized aluminum coating including an aluminum plating layer on an Al6061 article. In this example, the aluminum plating layer is applied via electroplating, and the anodization occurs in an oxalic acid bath. The anodized aluminum plating layer on the Al6061 article shows the lowest levels of impurities.















TABLE A











Anodized



RL



Al
Al



(detection



Plating
Plating



limit of

Al
Anodized
on
on


Parameter
test)
Units
6061
Al 6061
Al6061
Al6061





















Chromium
0.02
ppm
850
1600
1.7





(μg/g)






Copper
0.02
ppm
2500
2800
12
4




(μg/g)






Iron
0.05
ppm
1300
2700
140
26




(μg/g)






Magnesium
0.01
ppm
4200
9700
3.6
1.5




(μg/g)






Manganese
0.01
ppm
210
540
2.9
3.6




(μg/g)






Nickel
0.01
ppm
37
120
12
3




(μg/g)






Titanium
0.01
ppm
190
160

1.2




(μg/g)






Zinc
0.04
ppm
1000
1600
4.8





(μg/g)










FIG. 4 is a flow chart showing a method 400 for manufacturing an aluminum coated article, in accordance with embodiments of the present disclosure. The operations of process 400 may be performed by various manufacturing machines, as set forth in FIG. 1. The process 400 may be applied to coat aluminum any article.


At block 401, an article (e.g., an article having at least a conductive portion) is provided. For example, the article can be a conductive article formed of an aluminum alloy (e.g., Al 6061), another alloy, a metal, a metal oxide, or a ceramic. The article can be a shower head, a cathode sleeve, a sleeve liner door, a cathode base, a chamber liner, an electrostatic chuck base, etc., for use in a processing chamber.


At block 403, the article is prepared for coating, according to one embodiment. The surface of the article may be altered by roughening, smoothing, or cleaning the surface.


At block 405, the article is coated (e.g., plated) with aluminum. For example, the article can be electroplated with aluminum, as similarly described with respect to FIG. 2. In other examples, the coating can be applied by physical vapor deposition (PVD), chemical vapor deposition (CVD), twin wire arc spray, ion vapor deposition, sputtering, and cold spray.


At block 407, the article with the aluminum coating is cleaned, according to one embodiment. For example, the article can be cleaned by immersing the article in nitric acid to remove surface oxidation.


At block 409, the article with the aluminum coating is anodized, according to one embodiment. For example, the article can be anodized in a bath of oxalic acid or sulfuric acid, as similarly described with respect to FIG. 3.



FIG. 5 illustrates a scanning electron micrograph 500 of a cross-sectional view of an Al6061 article 501 with an aluminum coating 503, applied via electroplating at approximately 1000-fold magnification with a 50 micron scale shown. The thickness of the aluminum plating layer is about 70 microns.



FIG. 6 illustrates a scanning electron micrograph 600 of a cross-sectional view of an Al6061 article 601 with an aluminum coating 603, applied via electroplating, and an anodization layer 605, formed in an oxalic acid bath, at about 800-fold magnification with a 20 micron scale shown. The thickness of the aluminum plating layer is about 55 microns, and the thickness of the anodization layer is about 25 microns.


The preceding description sets forth numerous specific details such as examples of specific systems, components, methods, and so forth, in order to provide a good understanding of several embodiments of the present disclosure. It will be apparent to one skilled in the art, however, that at least some embodiments of the present disclosure may be practiced without these specific details. In other instances, well-known components or methods are not described in detail or are presented in simple block diagram format in order to avoid unnecessarily obscuring the present disclosure. Thus, the specific details set forth are merely exemplary. Particular implementations may vary from these exemplary details and still be contemplated to be within the scope of the present 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 phrase “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily all referring to the same embodiment. In addition, the term “or” is intended to mean an inclusive “or” rather than an exclusive “or.”


Although the operations of the methods herein are shown and described in a particular order, the order of the operations of each method may be altered so that certain operations may be performed in an inverse order or so that certain operation may be performed, at least in part, concurrently with other operations. In another embodiment, instructions or sub-operations of distinct operations may be in an intermittent and/or alternating manner.


It is to be understood that the above description is intended to be illustrative, and not restrictive. Many other embodiments will be apparent to those of skill in the art upon reading and understanding the above description. The scope of the disclosure should, therefore, be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled.

Claims
  • 1. A chamber component for a processing chamber, comprising: a body that comprises impurities;an aluminum coating on a surface of the body, wherein the aluminum coating is substantially free from impurities; andan anodization layer over the aluminum coating, wherein the anodization layer comprises Al2O3, and wherein the anodization layer further comprises: a dense barrier layer portion; anda porous columnar layer portion, wherein the porous columnar layer portion of the anodization layer has a porosity of about 40% to 50% and comprises a plurality of columnar nanopores, wherein the plurality of columnar nanopores have a diameter of 10 nm to 150 nm, and wherein a surface roughness of the anodization layer is about 40 micro-inch.
  • 2. The chamber component of claim 1, wherein the chamber component is a chamber component of a processing chamber that performs plasma processes.
  • 3. The chamber component of claim 1, wherein the aluminum coating has a thickness in a range of about 0.8 mils to about 5 mils.
  • 4. The chamber component of claim 1, wherein the anodization layer has a thickness of about 2-4 mils.
  • 5. The chamber component of claim 1, wherein the anodization layer has a thickness in a range from about 0.4 mils to about 4 mils.
  • 6. The chamber component of claim 1, wherein a thickness of the anodization layer is 2-3 times a thickness of the aluminum coating.
  • 7. The chamber component of claim 1, wherein the anodization layer has a thickness in a range from about 30% to less than 50% of the thickness of the aluminum coating.
  • 8. The chamber component of claim 1, wherein the anodization layer has a thickness in a range from about 40% to 60% of the thickness of the aluminum coating.
  • 9. The chamber component of claim 1, wherein the body comprises an alloy of at least one of copper or magnesium.
  • 10. The chamber component of claim 1, wherein the body comprises aluminum alloy, Al 6061.
  • 11. The chamber component of claim 1, wherein the body comprises a ceramic material.
  • 12. The chamber component of claim 1, wherein the body comprises a metal oxide.
  • 13. The chamber component of claim 1, wherein the anodization layer consists essentially of Al2O3.
  • 14. The chamber component of claim 13, wherein the anodization layer comprises at least one of: copper impurities at a concentration of approximately 4 parts per million (ppm);iron impurities at a concentration of approximately 26 ppm;magnesium impurities at a concentration of approximately 1.5 ppm;manganese impurities at a concentration of approximately 3.6 ppm;nickel impurities at a concentration of approximately 3 ppm;titanium impurities at a concentration of approximately 1.2 ppm;chromium impurities at a concentration of approximately 0 ppm; andzinc impurities at a concentration of approximately 0 ppm.
  • 15. The chamber component of claim 1, wherein the chamber component is selected from a group consisting of a showerhead, a cathode sleeve, a sleeve liner door, a cathode base, a chamber liner, and an electrostatic chuck base.
  • 16. The chamber component of claim 1, wherein the plurality of columnar nanopores have a diameter of about 20-30 nm.
  • 17. A chamber component for a processing chamber, comprising: a body that comprises impurities;an aluminum coating on a surface of the body, wherein the aluminum coating is substantially free from impurities; andan anodization layer over the aluminum coating, wherein the anodization layer comprises Al2O3, and wherein the anodization layer further comprises: a dense barrier layer portion; anda porous columnar layer portion, wherein the porous columnar layer portion of the anodization layer has a porosity of about 40% to 70% and comprises a plurality of columnar nanopores, wherein the plurality of columnar nanopores have a diameter of 10 nm to 150 nm, and wherein a surface roughness of the anodization layer is about 40 micro-inch.
  • 18. The chamber component of claim 17, wherein the anodization layer has a thickness of about 2-4 mils and the aluminum coating has a thickness in a range of about 0.8 mils to about 4 mils.
RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 14/762,151, filed Jul. 20, 2015, which is a U.S. National Stage Application under 35 U.S.C. § 371 of International PCT Application No. PCT/US2014/019999, filed Mar. 4, 2014, which claims priority to U.S. Provisional Application No. 61/783,667, filed Mar. 14, 2013, all of which are hereby incorporated by reference herein.

US Referenced Citations (79)
Number Name Date Kind
3151948 Steeves Oct 1964 A
3969195 Dotzer et al. Jul 1976 A
4430387 Nakagawa et al. Feb 1984 A
4465561 Nguyen et al. Aug 1984 A
4624752 Arrowsmith et al. Nov 1986 A
4883541 Tadros Nov 1989 A
4925738 Tsuya et al. May 1990 A
4948475 Doetzer et al. Aug 1990 A
5069938 Lorimer et al. Dec 1991 A
5104514 Quartarone Apr 1992 A
5192610 Lorimer et al. Mar 1993 A
5494713 Ootuki Feb 1996 A
5779848 Aruga Jul 1998 A
6027629 Hisamoto et al. Feb 2000 A
6444304 Hisamoto et al. Sep 2002 B1
6466881 Shih et al. Oct 2002 B1
6521046 Tanaka et al. Feb 2003 B2
6659331 Thach et al. Dec 2003 B2
6682627 Shamouilian et al. Jan 2004 B2
6686053 Wada et al. Feb 2004 B2
6776873 Sun et al. Aug 2004 B1
7005194 Wada et al. Feb 2006 B2
7033447 Lin et al. Apr 2006 B2
7048814 Lin et al. May 2006 B2
7055732 Thach et al. Jun 2006 B2
7732056 Bhatnagar et al. Jun 2010 B2
8067067 Sun et al. Nov 2011 B2
8124240 Ohmi et al. Feb 2012 B2
8128750 Kenworthy et al. Mar 2012 B2
8129029 Sun et al. Mar 2012 B2
8206833 Ohmi et al. Jun 2012 B2
8282987 Kenworthy et al. Oct 2012 B2
8591986 Ajdelsztajn et al. Nov 2013 B1
8999475 Mitsuhashi Apr 2015 B2
9012030 Han et al. Apr 2015 B2
9123651 Shih et al. Sep 2015 B2
9337002 Daugherty et al. May 2016 B2
9528176 Mizuno et al. Dec 2016 B2
9663870 Sun et al. May 2017 B2
20030044714 Teraoka et al. Mar 2003 A1
20030047464 Sun et al. Mar 2003 A1
20030056897 Shamouilian et al. Mar 2003 A1
20040124280 Shih et al. Jul 2004 A1
20040126499 Heinrich et al. Jul 2004 A1
20040137299 Mazza et al. Jul 2004 A1
20040221959 Choi et al. Nov 2004 A1
20050037193 Sun et al. Feb 2005 A1
20060019035 Munz et al. Jan 2006 A1
20060024517 Doan et al. Feb 2006 A1
20060060472 Tomita et al. Mar 2006 A1
20060093736 Raybould et al. May 2006 A1
20060234396 Tomita et al. Oct 2006 A1
20070012657 O'Donnell et al. Jan 2007 A1
20080029032 Sun et al. Feb 2008 A1
20080223725 Han et al. Sep 2008 A1
20080241517 Kenworthy et al. Oct 2008 A1
20080283408 Nishizawa Nov 2008 A1
20090050485 Wada et al. Feb 2009 A1
20090145769 Tsuda Jun 2009 A1
20090298251 Choi et al. Dec 2009 A1
20100155251 Bogue et al. Jun 2010 A1
20100170937 Calla Jul 2010 A1
20110020665 Serafin et al. Jan 2011 A1
20110168210 Tabata et al. Jul 2011 A1
20110206833 Sexton et al. Aug 2011 A1
20110220289 Tanaka et al. Sep 2011 A1
20120103526 Ouye et al. May 2012 A1
20120138472 Han et al. Jun 2012 A1
20120247961 Ohmi et al. Oct 2012 A1
20130008796 Silverman et al. Jan 2013 A1
20140110145 Elie et al. Apr 2014 A1
20140120312 He et al. May 2014 A1
20140272459 Daugherty et al. Sep 2014 A1
20140315392 Xu et al. Oct 2014 A1
20150064450 Sun et al. Mar 2015 A1
20150203981 Mitsuhashi Jul 2015 A1
20150337450 Shih et al. Nov 2015 A1
20150376810 Browning et al. Dec 2015 A1
20160002811 Sun et al. Jan 2016 A1
Foreign Referenced Citations (10)
Number Date Country
102864479 Jan 2013 CN
10248118 Apr 2004 DE
0792951 Sep 2001 EP
H05129467 May 1993 JP
2009-099853 May 2009 JP
100607790 Aug 2006 KR
10-2006-0111201 Oct 2006 KR
10-2007-0001722 Jan 2007 KR
10-2012-0077375 Jul 2012 KR
2009031841 Dec 2009 WO
Non-Patent Literature Citations (4)
Entry
International Search Report and Written Opinion dated Jun. 25, 2014 for PCT/US2014/019999 filed Mar. 3, 2014.
Ohgai et al., “Template Synthesis and Magnetoresistance Property of Ni and Co Single Nanowires Electrodeposited into nanopores with a Wide Range of Aspect Ratios,” J. Phys. D: Appl. Phys., Nov. 25, 2003, vol. 36, pp. 3109-3114.
Tan et al., “High Aspect Ratio Microstructures on Porous Anodic Aluminum Oxide,” IEEE, Jan. 1995, pp. 267-272.
Paredes et al., “The Effect of Roughness and Pre-Heating of the Substrate on the Morphology of Aluminum Coatings Deposited by Thermal Spraying,” Surface & Coatings Technology, Sep. 8, 2005, vol. 200, pp. 3049-3055.
Related Publications (1)
Number Date Country
20180066373 A1 Mar 2018 US
Provisional Applications (1)
Number Date Country
61783667 Mar 2013 US
Divisions (1)
Number Date Country
Parent 14762151 US
Child 15811563 US