The present disclosure relates generally to hermetic barrier layers, and more particularly to methods and compositions used to seal solid structures using low melting temperature glasses.
Hermetic barrier layers can be used to protect sensitive materials from deleterious exposure to a wide variety of liquids and gases. As used herein, “hermetic” refers to a state of being completely or substantially sealed, especially against the escape or entry of water or air, though protection from exposure to other liquids and gases is contemplated.
Glass-to-glass bonding techniques can be used to sandwich a workpiece between adjacent substrates and generally provide a degree of encapsulation. Conventionally, glass-to-glass substrate bonds such as plate-to-plate sealing techniques are performed with organic glues or inorganic glass frits. Device makers of systems requiring thoroughly hermetic conditions for long-term operation generally prefer inorganic metal, solder, or frit-based sealing materials because organic glues (polymeric or otherwise) form barriers that are generally permeable to water and oxygen at levels many orders of magnitude greater than the inorganic options. On the other hand, while inorganic metal, solder, or frit-based sealants can be used to form impermeable seals, the resulting sealing interface is generally opaque as a result of the metal cation composition, scattering from gas bubble formation, and distributed ceramic-phase constituents.
Frit-based sealants, for instance, include glass materials that have been ground to a particle size ranging typically from about 2 to 150 microns. For frit-sealing applications, the glass frit material is typically mixed with a negative CTE material having a similar particle size, and the resulting mixture is blended into a paste using an organic solvent. Example negative CTE inorganic fillers include cordierite particles (e.g. Mg2Al3 [AlSi5O18]) or barium silicates. The solvent is used to adjust the viscosity of the mixture.
To join two substrates, a glass frit layer can be applied to sealing surfaces on one or both of the substrates by spin-coating or screen printing. The frit-coated substrate(s) are initially subjected to an organic burn-out step at relatively low temperature (e.g., 250° C. for 30 minutes) to remove the organic vehicle. Two substrates to be joined are then assembled/mated along respective sealing surfaces and the pair is placed in a wafer bonder. A thermo-compressive cycle is executed under well-defined temperature and pressure whereby the glass frit is melted to form a compact glass seal.
Glass frit materials, with the exception of certain lead-containing compositions, typically have a glass transition temperature greater than 450° C. and thus require processing at elevated temperatures to form the barrier layer. Such a high-temperature sealing process may be detrimental to temperature-sensitive workpieces.
Further, the negative CTE inorganic fillers, which are used in order to lower the thermal expansion coefficient mismatch between typical substrates and the glass frit, will be incorporated into the bonding joint and result in a frit-based barrier layer that is neither transparent nor translucent.
Based on the foregoing, it would be desirable to form glass-to-glass seals at low temperatures that are transparent and optionally hermetic.
Disclosed herein are methods for forming a laser-sealed interface between opposing glass substrates using a low melting temperature glass (low Tg) sealing material at the interface. Embodiments of the method involve temporary absorption of laser radiation and the concomitant localized melting of both the glass sealing material and the glass substrates to affect the seal. After the seal is formed and the materials are cooled, the resulting package is transparent.
A method of protecting a workpiece comprises forming a low Tg glass sealing layer over a major surface of a first glass substrate, arranging a workpiece to be protected between the first substrate and a second substrate where the sealing layer is in contact with the second substrate, and locally heating the glass sealing layer and the glass substrates with laser radiation to melt the sealing layer and the glass substrates to form a glass seal between the substrates. Absorption of the laser radiation by the glass substrates is transient and thermally-induced.
The laser radiation can be translated to define a sealing interface that can cooperate with the glass substrates to define a hermetic package for the workpiece. Example workpieces include quantum dots. Example laser radiation includes ultra-violet (UV) radiation.
Additional features and advantages will be set forth in the detailed description which follows, and in part will be readily apparent to those skilled in the art from that description or recognized by practicing the invention as described herein, including the detailed description which follows, the claims, as well as the appended drawings.
It is to be understood that both the foregoing general description and the following detailed description present embodiments of the invention, and are intended to provide an overview or framework for understanding the nature and character of the invention as it is claimed. The accompanying drawings are included to provide a further understanding of the invention, and are incorporated into and constitute a part of this specification. The drawings illustrate various embodiments of the invention and together with the description serve to explain the principles and operations of the invention.
Although the sealing techniques disclosed herein are described in certain embodiments with respect to manufacturing a hermetically-sealed OLED display, it should be understood that the same or similar sealing techniques can be used to seal two glass plates to one another that can be used in a wide variety of applications and devices. Accordingly, the sealing techniques of the present disclosure should not be construed in a limited manner. For example, thin film sensors and vacuum-insulated glass windows may be fabricated using the present methods.
A sealed structure comprises opposing glass substrates and a low melting temperature glass sealing layer formed at an interface between the substrates. A laser is used to locally heat the sealing material as well as the respective substrates to affect the seal. During sealing, the sealing material melts and re-solidifies to form the seal. In embodiments, material from one or both of the substrates also melts and re-solidifies in a region proximate the melted and re-solidified sealing material. In such embodiments, the substrate material may constitute a portion of the sealed interface, resulting in a glass-to-glass weld.
In embodiments, the glass substrates exhibit transient absorption of the incident laser radiation. Initial absorption by the sealing glass melts the sealing glass material and, due principally to a local increase in temperature of the glass substrate, induces a temporary absorption of the laser radiation by the glass substrate, which may cause localized melting of the substrates. Absorption by the glass substrates decays after the sealing process is complete, resulting in an optically-transparent seal.
Transient absorption as used herein refers generally to any light-material interaction involving additional absorption of light from light-induced defects, to include color center formation. A feature of transient absorption is that additional absorption occurs in the material at excitation wavelengths above and beyond simple linear absorption. Thus, in various embodiments, temporary absorption of laser radiation by a glass substrate can occur by increasing the temperature of the substrate material. Transient absorption may include multi-photon processes.
In contrast to pico-second pulse width, purely non-linear absorption phenomena observed in some glass materials, the methods described herein involve non-linear absorption of the glass substrate materials at relatively long (1-10 ns) laser pulses. Typical power densities for 355 nm lasers, for instance, operating at a repetition rate of about 30 kHz are about 0.5 to 1 MW/cm2.
As used herein, the term “induced absorption” refers to the absolute value of the difference in internal transmission per centimeter of the glass upon exposure to laser irradiation. Of particular interest is the induced absorption at about 355 nm, which means the induced absorption at 355 nm upon exposure to an excimer laser operating at about 355 nm for 10 billion pulses at about 70 μJ/(pulse·cm2).
Thus, in embodiments, laser radiation incident on a glass substrate/sealing glass/glass substrate interface can initially be absorbed by the sealing glass material inducing melt formation and, in turn, cause a local increase in temperature which temporarily alters the absorption characteristics of the adjacent glass substrate material. A temperature increase in glass substrate material can occur through heat conduction from the sealing glass and via a temperature-induced absorption enhancement from the illumination. Transient absorption of the laser radiation by the glass substrate can cause local melting of the glass substrate material in addition to local melting of the sealing glass, forming a glass-to-glass seal. Eagle 2000® glass, for example, softens at a temperature of about 830° C. When the laser radiation is removed and the sealed area cooled, the absorption characteristics of the glass substrate material return to their pre-processed state, i.e., optically transparent.
The integrity of the seal and its strength is maintained by slow cooling (self-annealing) of the substrate glass and the attendant color center relaxation, as well as by the relative thinness of the low melting temperature sealing glass, which minimizes the impact of any CTE mismatch. Further minimizing the CTE mismatch in the sealed region is the inter-diffusion of the mismatched materials within the weld zone, which effectively dilutes the expansion mismatch.
The present method can be used to form a hermetically-sealed package. In further embodiments, the method can be used to form spot seals for non-hermetic glass packages.
A method of forming an encapsulated workpiece according to one embodiment is illustrated schematically in
A focused laser beam 501 from laser 500 can be used to locally melt the low melting temperature glass and adjacent glass substrate material form a sealed interface. In one approach, the laser can be focused through the first substrate 302 and then translated (scanned) across the sealing surface to locally heat the glass sealing material. In order to affect local melting of the glass layer, the glass layer is preferably absorbing at the laser processing wavelength. The glass substrates can be initially transparent (e.g., at least 50%, 70%, 80% or 90% transparent) at the laser processing wavelength.
In an alternate embodiment, in lieu of forming a patterned glass layer, a blanket layer of sealing (low melting temperature) glass can be formed over substantially all of a surface of a first substrate. An assembled structure comprising the first substrate/sealing glass layer/second substrate can be assembled as above, and a laser can be used to locally-define the sealing interface between the two substrates.
Laser 500 can have any suitable output to affect sealing. An example laser is a UV laser such as a 355 nm laser, which lies in the range of transparency for common display glasses. A suitable laser power can range from about 5 W to about 6.15 W.
The width of the sealed region, which can be proportional to the laser spot size, can be about 0.1 to 2 mm, e.g., 0.1, 0.2, 0.5, 1, 1.5 or 2 mm. A translation rate of the laser (i.e., sealing rate) can range from about 1 mm/sec to 100 mm/sec, such as 1, 2, 5, 10, 20, 50 or 100 mm/sec. The laser spot size (diameter) can be about 0.5 to 1 mm.
Suitable glass substrates exhibit significant induced absorption during sealing. In embodiments, first substrate 302 is a transparent glass plate like the ones manufactured and marketed by Corning Incorporated under the brand names of Code 1737 glass or Eagle 2000® glass. Alternatively, first substrate 302 can be any transparent glass plate such as, for example, the ones manufactured and marketed by Asahi Glass Co. (e.g., AN100 glass), Nippon Electric Glass Co., (e.g., OA-10 glass or OA-21 glass), or Samsung Corning Precision Glass Co. Second substrate 304 may be the same glass material as the first glass substrate, or second substrate 304 may be a non-transparent substrate. The glass substrates can have a coefficient of thermal expansion of less than about 150×10−7/° C., e.g., less than 50×10−7, 20×10−7 or 10×10−7/° C.
A plot of transmission versus wavelength for various display glass substrates is shown in
The temperature dependence of the UV absorption edge for silica glass is illustrated in
Shown in
In embodiments, absorption at room temperature of a laser processing wavelength by the glass substrates is less than 15%. However, absorption at elevated temperatures (e.g., greater than 400° C.) of a laser processing wavelength by the glass substrates is greater than 15%. In embodiments, absorption by the glass substrate material increases, for example, to values of 20, 30, 40, 50, 60% or more as the temperature of the glass substrate increases. During sealing, the glass substrate temperature proximate to the sealing interface can increase to at least 400, 500, 600, 700 or 800° C.
In various embodiments of the present disclosure, the glass sealing materials and resulting layers are transparent and/or translucent, thin, impermeable, “green,” and configured to form hermetic seals at low temperatures and with sufficient seal strength to accommodate large differences in CTE between the sealing material and the adjacent glass substrates. In embodiments, the sealing layers are free of fillers. In further embodiments, the sealing layers are free of binders. In still further embodiments, the sealing layers are free of fillers and binders. Further, organic additives are not used to form the hermetic seal. The low melting temperature glass materials used to form the sealing layer(s) are not frit-based or powders formed from ground glasses. In embodiments, the sealing layer material is a low Tg glass that has a substantial optical absorption cross-section at a predetermined wavelength which matches or substantially matches the operating wavelength of a laser used in the sealing process.
In embodiments, absorption at room temperature of a laser processing wavelength by the low Tg glass layer is at least 15%.
In general, suitable sealant materials include low Tg glasses and suitably reactive oxides of copper or tin. The glass sealing material can be formed from low Tg materials such as phosphate glasses, borate glasses, tellurite glasses and chalcogenide glasses. As defined herein, a low Tg glass material has a glass transition temperature of less than 400° C., e.g., less than 350, 300, 250 or 200° C.
Example borate and phosphate glasses include tin phosphates, tin fluorophosphates and tin fluoroborates. Sputtering targets can include such glass materials or, alternatively, precursors thereof. Example copper and tin oxides are CuO and SnO, which can be formed from sputtering targets comprising pressed powders of these materials.
Optionally, the glass sealing compositions can include one or more dopants, including but not limited to tungsten, cerium and niobium. Such dopants, if included, can affect, for example, the optical properties of the glass layer, and can be used to control the absorption by the glass layer of laser radiation. For instance, doping with ceria can increase the absorption by a low Tg glass barrier at laser processing wavelengths.
Example tin fluorophosphate glass compositions can be expressed in terms of the respective compositions of SnO, SnF2 and P2O5 in a corresponding ternary phase diagram. Suitable tin fluorophosphates glasses include 20-100 mol % SnO, 0-50 mol % SnF2 and 0-30 mol % P2O5. These tin fluorophosphates glass compositions can optionally include 0-10 mol % WO3, 0-10 mol % CeO2 and/or 0-5 mol % Nb2O5.
For example, a composition of a doped tin fluorophosphate starting material suitable for forming a glass sealing layer comprises 35 to 50 mole percent SnO, 30 to 40 mole percent SnF2, 15 to 25 mole percent P2O5, and 1.5 to 3 mole percent of a dopant oxide such as WO3, CeO2 and/or Nb2O5.
A tin fluorophosphate glass composition according to one particular embodiment is a niobium-doped tin oxide/tin fluorophosphate/phosphorus pentoxide glass comprising about 38.7 mol % SnO, 39.6 mol % SnF2, 19.9 mol % P2O5 and 1.8 mol % Nb2O5. Sputtering targets that can be used to form such a glass layer may include, expressed in terms of atomic mole percent, 23.04% Sn, 15.36% F, 12.16% P, 48.38% O and 1.06% Nb.
A tin phosphate glass composition according to an alternate embodiment comprises about 27% Sn, 13% P and 60% O, which can be derived from a sputtering target comprising, in atomic mole percent, about 27% Sn, 13% P and 60% O. As will be appreciated, the various glass compositions disclosed herein may refer to the composition of the deposited layer or to the composition of the source sputtering target.
As with the tin fluorophosphates glass compositions, example tin fluoroborate glass compositions can be expressed in terms of the respective ternary phase diagram compositions of SnO, SnF2 and B2O3. Suitable tin fluoroborate glass compositions include 20-100 mol % SnO, 0-50 mol % SnF2 and 0-30 mol % B2O3. These tin fluoroborate glass compositions can optionally include 0-10 mol % WO3, 0-10 mol % CeO2 and/or 0-5 mol % Nb2O5.
Additional aspects of suitable low Tg glass compositions and methods used to form glass sealing layers from these materials are disclosed in commonly-assigned U.S. Pat. No. 5,089,446 and U.S. patent application Ser. Nos. 11/207,691, 11/544,262, 11/820,855, 12/072,784, 12/362,063, 12/763,541 and 12/879,578, the entire contents of which are incorporated by reference herein.
A total thickness of a glass sealing layer can range from about 100 nm to 10 microns. In various embodiments, a thickness of the layer can be less than 10 microns, e.g., less than 10, 5, 2, 1, 0.5 or 0.2 microns. Example glass sealing layer thicknesses include 0.1, 0.2, 0.5, 1, 2, 5 or 10 microns.
According to embodiments, the choice of the sealing layer material and the processing conditions for forming a sealing layer over a glass substrate are sufficiently flexible that the substrate is not adversely affected by formation of the glass layer.
Low melting temperature glasses can be used to seal or bond different types of substrates. Sealable and/or bondable substrates include glasses, glass-glass laminates, glass-polymer laminates, glass-ceramics or ceramics, including gallium nitride, quartz, silica, calcium fluoride, magnesium fluoride or sapphire substrates. In embodiments, one substrate can be a phosphor-containing glass plate, which can be used, for example, in the assembly of a light emitting device.
Glass substrates can have any suitable dimensions. Substrates can have areal (length and width) dimensions that independently range from 1 cm to 5 m (e.g., 0.1, 1, 2, 3, 4 or 5 m) and a thickness dimension that can range from about 0.5 mm to 2 mm (e.g., 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.2, 1.5 or 2 mm) In further embodiments, a substrate thickness can range from about 0.05 mm to 0.5 mm (e.g., 0.05, 0.1, 0.2, 0.3, 0.4 or 0.5 mm) In still further embodiments, a glass substrate thickness can range from about 2 mm to 10 mm (e.g., 2, 3, 4, 5, 6, 7, 8, 9 or 10 mm).
A phosphor-containing glass plate, for example, comprising one or more of a metal sulfide, metal silicate, metal aluminate or other suitable phosphor, can be used as a wavelength-conversion plate in white LED lamps. White LED lamps typically include a blue LED chip that is formed using a group III nitride-based compound semiconductor for emitting blue light. White LED lamps can be used in lighting systems, or as backlights for liquid crystal displays, for example. The low melting temperature glasses and associate sealing method disclosed herein can be used to seal or encapsulate the LED chip.
Hermetic encapsulation of a workpiece using the disclosed materials and methods can facilitate long-lived operation of devices otherwise sensitive to degradation by oxygen and/or moisture attack. Example workpieces, devices or applications include flexible, rigid or semi-rigid organic LEDs, OLED lighting, OLED televisions, photovoltaics, MEMs displays, electrochromic windows, fluorophores, alkali metal electrodes, transparent conducting oxides, quantum dots, etc.
As used herein, a hermetic layer is a layer which, for practical purposes, is considered substantially airtight and substantially impervious to moisture and/or oxygen. By way of example, the hermetic seal can be configured to limit the transpiration (diffusion) of oxygen to less than about 10−2 cm3/m2/day (e.g., less than about 10−3 cm3/m2/day), and limit the transpiration (diffusion) of water to about 10−2 g/m2/day (e.g., less than about 10−3, 10−4, 10−5 or 10−6 g/m2/day). In embodiments, the hermetic seal substantially inhibits air and water from contacting a protected workpiece.
A simplified schematic showing a portion of an LED assembly is depicted in
One component of the LED assembly 900 is a quantum dot sub-assembly 960, which in various embodiments includes a plurality of quantum dots 950 disposed between an upper plate 962a, 962b and a lower plate 964. The quantum dots in
A thermo-compressive stress may be applied to affect sealing between the upper and lower plates, or the interface(s) may be laser sealed by focusing a suitable laser on or near the glass layer(s) through either of the upper or lower plates.
A further component of the LED assembly 900 is an emitter 920 with a wavelength-conversion plate 940 formed over an output of the emitter. The emitter 920 can include a semiconductor material such as a gallium nitride wafer, and the wavelength-conversion plate 940 can comprise a glass or ceramic having particles of a phosphor embedded or infiltrated therein. In embodiments, a low melting temperature glass can be used to directly bond a sealing surface of the wavelength-conversion plate to a sealing surface of the emitter.
Alternate embodiments, which include example photovoltaic (PV) device or organic light emitting diode (OLED) device architectures, are depicted in
Illustrated in
To form a seal or bond between respective sealing surfaces, initially a glass layer may be formed on one or both of the surfaces. In one embodiment, a glass layer is formed over each of the surfaces to be bonded, and after the surfaces are brought together, a focused laser is used to melt the glass layers and the adjacent sealing surface material to create the seal. In one further embodiment, a glass layer is formed over only one of the surfaces to be bonded, and after the glass-coated surface and non-glass-coated surface are brought together, a focused laser is used to locally melt the glass layer and the respective surfaces to be bonded to create the seal.
A method of bonding two substrates comprises forming a first glass layer on a sealing surface of a first substrate, forming a second glass layer on a sealing surface of a second substrate, placing at least a portion of the first glass layer in physical contact with at least a portion of the second glass layer, and heating the glass layers to locally melt the glass layers and the sealing surfaces to form a glass-to-glass weld between the first and second substrates.
In alternate embodiments, the sealing approaches disclosed herein can be used to form vacuum-insulated glass (VIG) windows where the previously-discussed active components (such as the emitter, collector or quantum dot architecture) are omitted from the structure, and a low melting temperature glass layer is used to seal respective bonding interfaces between opposing glass panes in a multi-pane window. A simplified VIG window architecture is shown in
In each of the sealing architectures disclosed herein, sealing using a low melting temperature glass layer may be accomplished by the local heating, melting and then cooling of both the glass layer and the glass substrate material located proximate to the sealing interface.
As used herein, the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to a “glass substrate” includes examples having two or more such “glass substrates” unless the context clearly indicates otherwise.
Ranges can be expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, examples include from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another aspect. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint.
Unless otherwise expressly stated, it is in no way intended that any method set forth herein be construed as requiring that its steps be performed in a specific order. Accordingly, where a method claim does not actually recite an order to be followed by its steps or it is not otherwise specifically stated in the claims or descriptions that the steps are to be limited to a specific order, it is no way intended that any particular order be inferred.
It is also noted that recitations herein refer to a component being “configured” or “adapted to” function in a particular way. In this respect, such a component is “configured” or “adapted to” embody a particular property, or function in a particular manner, where such recitations are structural recitations as opposed to recitations of intended use. More specifically, the references herein to the manner in which a component is “configured” or “adapted to” denotes an existing physical condition of the component and, as such, is to be taken as a definite recitation of the structural characteristics of the component.
It will be apparent to those skilled in the art that various modifications and variations can be made to the present invention without departing from the spirit and scope of the invention. Since modifications, combinations, sub-combinations and variations of the disclosed embodiments incorporating the spirit and substance of the invention may occur to persons skilled in the art, the invention should be construed to include everything within the scope of the appended claims and their equivalents.
This application claims the benefit of priority under 35 U.S.C. §119 of U.S. Provisional Application Ser. No. 61/731,784 filed on Nov. 30, 2012, the content of which is relied upon and incorporated herein by reference in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
5089446 | Cornelius et al. | Feb 1992 | A |
5272309 | Goruganthu et al. | Dec 1993 | A |
5489321 | Tracy | Feb 1996 | A |
6423613 | Geusic | Jul 2002 | B1 |
6501043 | Ruben | Dec 2002 | B1 |
6501044 | Klockhaus et al. | Dec 2002 | B1 |
6717100 | Ruben | Apr 2004 | B2 |
6762072 | Lutz | Jul 2004 | B2 |
6818530 | Shimoda et al. | Nov 2004 | B2 |
7344901 | Hawtof | Mar 2008 | B2 |
7361573 | Takayama et al. | Apr 2008 | B2 |
7449773 | Tarn | Nov 2008 | B2 |
7615506 | Aitken | Nov 2009 | B2 |
7626138 | Bovatsek et al. | Dec 2009 | B2 |
7722929 | Aitken et al. | May 2010 | B2 |
7829147 | Aitken et al. | Nov 2010 | B2 |
7872338 | Tarn | Jan 2011 | B2 |
8134293 | Logunov et al. | Mar 2012 | B2 |
8148179 | Aitken | Apr 2012 | B2 |
8314359 | Bovatsek et al. | Nov 2012 | B2 |
8343412 | Klein et al. | Jan 2013 | B2 |
8367440 | Takayama et al. | Feb 2013 | B2 |
8375744 | Becken et al. | Feb 2013 | B2 |
8389891 | Bovatsek et al. | Mar 2013 | B2 |
8490434 | Watanabe et al. | Jul 2013 | B2 |
8530786 | Bovatsek et al. | Sep 2013 | B2 |
8563113 | Edwards et al. | Oct 2013 | B2 |
8697242 | Kawanami et al. | Apr 2014 | B2 |
8778121 | Tuennermann et al. | Jul 2014 | B2 |
8778469 | Kawanami et al. | Jul 2014 | B2 |
8796109 | Ruben et al. | Aug 2014 | B2 |
8975159 | Akiyama | Mar 2015 | B2 |
9021836 | Matsumoto | May 2015 | B2 |
9093668 | Han | Jul 2015 | B2 |
9120287 | Ruben et al. | Sep 2015 | B2 |
9171721 | Danzl et al. | Oct 2015 | B2 |
20010027633 | Amako et al. | Oct 2001 | A1 |
20040082145 | Reichenbach et al. | Apr 2004 | A1 |
20040256367 | Ruben | Dec 2004 | A1 |
20050116245 | Aitken | Jun 2005 | A1 |
20050151151 | Hawtof et al. | Jul 2005 | A1 |
20050199599 | Li et al. | Sep 2005 | A1 |
20060172875 | Cortright | Aug 2006 | A1 |
20070040501 | Aitken et al. | Feb 2007 | A1 |
20090308105 | Pastel | Dec 2009 | A1 |
20100047587 | Itoh | Feb 2010 | A1 |
20100190051 | Aitken et al. | Jul 2010 | A1 |
20110209813 | Shibuya et al. | Sep 2011 | A1 |
20120028011 | An et al. | Feb 2012 | A1 |
20120147538 | Kawanami | Jun 2012 | A1 |
20120240632 | Matsumoto | Sep 2012 | A1 |
20130095260 | Bovatsek et al. | Apr 2013 | A1 |
20130112650 | Karam et al. | May 2013 | A1 |
20130125516 | Bayne et al. | May 2013 | A1 |
20130183474 | Bovatsek et al. | Jul 2013 | A1 |
20130223922 | Koval | Aug 2013 | A1 |
20140004318 | Bovatsek et al. | Jan 2014 | A1 |
20140087099 | Veerasamy et al. | Mar 2014 | A1 |
20140151742 | Logunov et al. | Jun 2014 | A1 |
20140242306 | Koval et al. | Aug 2014 | A1 |
20150027168 | Dabich, II et al. | Jan 2015 | A1 |
Number | Date | Country |
---|---|---|
1117502 | Jan 2003 | EP |
2012104397 | May 2012 | JP |
9602473 | Feb 1996 | WO |
0130530 | May 2001 | WO |
WO2008045249 | Apr 2008 | WO |
2013070791 | May 2013 | WO |
2013130374 | Sep 2013 | WO |
2014052178 | Apr 2014 | WO |
2014085427 | Jun 2014 | WO |
Entry |
---|
International Search Report and Written Opinion, dated Apr. 9, 2014, International Application No. PCT/US2013/071952, International Filing Date Nov. 26, 2013. |
Number | Date | Country | |
---|---|---|---|
20140151742 A1 | Jun 2014 | US |
Number | Date | Country | |
---|---|---|---|
61731784 | Nov 2012 | US |