The present invention relates generally to the field of solid-state lighting and more specifically to high efficiency phosphor-converted LEDs.
Solid-state lighting (SSL) is a type of lighting that does not use an electrical filament or a gas in the production of light. A primary advantage of SSL over conventional lighting technologies is the potential energy savings as a result of its higher luminous efficiencies over conventional lighting devices. For example, SSL is capable of 50% efficiency with 200 lumen per watt (lm/W) efficacy (compared to 15 lm/W for incandescents and 60-90 lm/W for fluorescents) and up to 100 khr lifetimes. This is approximately 100 times the lifetime of conventional incandescent bulbs and 10 times the lifetime of fluorescents. The Department of Energy (DOE) has set a goal of 50% electrical-to-optical system efficiency with a spectrum accurately reproducing the solar spectrum by 2020. The Optoelectronic Industry Development Association (OIDA) aims for 200-hm/W luminous efficiency with a color rendering index greater than 80.
Each of these conventional methods and devices has deficiencies. Color mixing is hindered by the absence of an efficient LED material in the 500 nm to 580 nm (green to-yellow) range. Wavelength conversion suffers from phosphor conversion loss and package designs that do not extract phosphor-converted light efficiently.
SSL devices primarily include light emitting diodes (LEDs), which include a small chip semiconductor, i.e. the LED source, mounted in a reflector cup on a lead frame. The LED source generates photons of light at a first wavelength when energized. The reflector cup reflects photons out of the LED. An optic, generally a silicone or epoxy encapsulation, aids in light extraction from the LED source and protects the LED components.
High efficiency generation of white light with LEDs has conventionally been according to one of three methods: 1) color mixing; 2) wavelength conversion; or 3) a combination of methods 1 and 2. Color mixing is the use of multiple LEDs across the visible spectrum (e.g. blue+green+red LEDs), which combine to produce a white light. Wavelength conversion is the use of a single, efficient, short wavelength LED emitting light at the first wavelength, which is then at least partially absorbed by a phosphor within the LED and re-emitted at a second wavelength. LEDs under method 2 are generally referred to as phosphor-converted LEDs (pcLEDs).
Conventional pcLEDs have generally two structural arrangements. First, the phosphor can encompass the LED source of the LED. The phosphor is typically a YAG:Ce crystalline powder in direct contact with the blue wavelength emitting LED source. Both are positioned upon a heat sink base and surrounded by an optic. The other arrangement is a scattered photon extraction (SPE) pcLED, which positions a planar phosphor-layer at a distance away from the LED source. Herein, the YAG:Ce phosphor, in powder form, creates a diffuse, semitransparent layer upon an acrylic optic with a planar surface.
When the phosphor is in direct contact with the LED source, the phosphor suffers from optical losses by reflection of phosphor-emission back into the LED source rather than through the optic and out of the LED. This can account for up to 60% of the total phosphor emission. The SPE pcLED suffers from scattering of the phosphor emissions. Scattering is the result of substantial differences in the indices of refraction of the phosphor powder and the material that encapsulates the phosphor (air, silicon, PMMA, or glass). The index of refraction, n, is a measure of the relative speed of light in a medium as compared to in a vacuum (where n.sub.vac=1). When light passes from one medium to another medium with a substantially different index of refraction, the speed and direction of the light changes and is known as refraction. Refraction can lead to a randomization, or scattering, of the directionality of the light. Scattering then reduces efficiency by increasing the path length (a) inside the phosphor layer by trapping of the emissions by total internal reflection and (b) inside the device package because of random directionality of the phosphor emission, both of which can lead to reabsorption and optical loss.
These phosphor-related deficiencies are then compounded by secondary losses encountered by other package design deficiencies, such as imperfections of the reflector cup within the LED. While the reflector cup is intended to direct the phosphor-emission out of the LED, internal reflections and path randomization can trap a portion of the phosphor-emission, such as between the reflector cup and the phosphor, and decrease LED efficiency by approximately 30%.
Thus, to reach the efficiency goals set forth by the DOE, the problems associated with package design must be eliminated by designing a high efficiency LED that resolves the issues identified above.
According to the embodiments of the present invention, a light emitting composite material is described. The light emitting composite material includes a glassy material and a plurality of phosphor particles suspended within the glassy material, wherein the refractive index of the plurality of phosphor particles is approximately equal to the refractive index of the glassy material.
The plurality of phosphor particles can be composed of an inorganic crystalline material selected from the group consisting of YxGdyAlvGawO12O:M3+, wherein x+y=3 and v+w=5; SrGaS4:M2+; SrS:M2+; X2Si5N8:M2+; and XSi2O2N2:M2+, wherein X is selected from the group consisting of He, Mg, Ca, Sr, and Ba and wherein M is selected from a group consisting of Ce, Eu, Mn, Nd, Pr, Sm, Gd, Tb, Dy, Ho, Br, Tm, Yb, Lu, Sc, Ti, V, Cr, Pe, Co, Ni, Cu, Zn, Ir, and Pt.
The glassy material can be an optical glass comprising an amount from 5% to about 35% of SiO2; an amount from about 55% to about 88% of PbO; optionally an amount less than 10% B2O3; optionally a combined amount less than 8% of Na2O and K2O; and optionally a combined amount less than about 15% total of TiO2, ZrO2, La2O3, ZnO, and BaO.
In other light emitting composites, the glassy material can be an optical glass comprising an amount from about 21% to about 30% of TIO2; an amount from about 30% to about 50% of BaO, NaO, BeO, CaO, SrO, CdO, Ga2O3, In2O3, or Y2O3; an amount from about 18% to about 24% of Al2O3; and an amount from about 1% to about 10% of SiO2, B2O3, PbO, GeO2, SnO2, ZrO2, HfO2, or ThO2.
In another aspect of the present invention, the light emitting composites of the present invention can be used within a phosphor-containing light emitting device (pcLED). The pcLED can be constructed as an Enhanced Light Extraction by Internal Reflection (ELIXIR) LED device.
In yet another aspect of the present invention, the light emitting composite can be used with a solid-state laser.
In yet another aspect of the present invention, the light emitting composite can be used as a luminescence collector.
Efficiency of a fully wavelength converted pcLED can be expressed as
ηpcL=ηLED·ηs·ηq·ηp Equation 1
where ηpcL is the total pcLED efficiency and is dependent upon the efficiency of the particular LED source, ηLED; the Stokes conversion efficiency, ·ηs, which is the quantum ratio of the average emission wavelengths of the LED and the phosphor; the phosphor quantum efficiency, ηq, which indicates the efficiency of the quantum conversion of light from a first wavelength to a second wavelength inside the phosphor; and the package efficiency, ·ηp, which is the efficiency of light extraction of LED- and phosphor-emitted photons from the LED device package. The product of ηq·ηp is the conversion efficiency (CE) for an LED device. The embodiments of the present invention optimize CE.
Package efficiency, ηp, of the present invention is improved over conventional LED devices by first separating an LED source 12 from first and second non-planar layers, wherein the second layer is composed of a phosphor 14, which will nearly eliminate the reflection of phosphor- and LED-emissions back into the LED source 12. Secondly, a planar reflector 16 is used to reduce the number of mirror reflections over the conventional LED. The result is an Enhanced Light eXtraction by Internal Reflection (ELIXIR) LED device 10, shown in
The ELIXIR LED 10 more specifically includes the first non-planar layer, i.e. a glass cover 18, surrounding and making immediate contact with the second non-planar layer, i.e. a phosphor 14, and a LED source 12 upon a heat sink base 20. The phosphor 14 and the LED source 12 are separated by a radius sufficient to substantially reduce the likelihood of phosphor-emissions reentering the LED source 12. This distance, r, is dependent upon a specified fraction of reentry, P, and is given by:
r≤√[A/(4·π·P)] Equation 2
Herein, A is the size of the LED source 12, i.e. the surface area of the LED chip. The high package efficiency is maintained as long as the proportions of the ELIXIR LED 10, namely the rphosphor/roptic ratio, are preserved, as described below in connection with
The LED source 12 can include any conventional resonance cavity LED or laser diode source generally emitting a light having a first wavelength ranging between about 350 nm to about 500 nm. This can include, but should not be limited to, a blue power LED with a peak wavelength of 455 nm with a 1000 mA DC drive capability.
The glass cover 18 can be any material suitable for the lens construction and for protection of the phosphor 14 and LED source 12, such as polymethyl methacrylate (PMMA) silicones, and glasses. In an alternative embodiment described herein, the glass cover 18 and the phosphor 14 may be made integral.
The phosphor 14 is applied to the glass cover 18 as a layer of inorganic phosphor crystalline powder. The phosphor 14 can be applied as a layer, for example, of about 100 μm in thickness, to an inner surface of the glass cover 18 from a solution of acetone or other solvent. The phosphor 14 should be selected such that the phosphor absorption band substantially overlaps with the LED-emission band, as shown in
Though not specifically shown, the glass cover 18 can be eliminated and the phosphor 14 is applied as a layer upon the inside radius of a hemispherical optic 22.
While the phosphor 14, glass cover 18, and optic 22 are generally illustrated and explained with a hemispherical shape, the shape should not be considered so limited. That is, the shape can include hemispheres (see
In optimizing TN of Equation 1 and the ELIXIR LED 10 of
Because of their large surface-to-volume ratio, nanoparticles have low quantum efficiencies. Thus, the inorganic crystalline 42 should be a particle 46 that is larger than about 10 nm, i.e. not a nanoparticle. However, because the light-emitting composite material 40 has a finite thickness, the inorganic crystalline 42 should be smaller than the thickness of the light-emitting composite material 40. Suitable inorganic crystalline 42 can include YxGdyAlvGawO12:M3+, wherein x+y=3 and v+w=5; SrGa2S4:M2+; SrS:M+; X2Si5N8:M2+; and XSi2O2N:M2+, wherein X is selected from a group consisting of Be, Mg, Ca, Sr, and Ba and wherein M is selected from a group consisting of Ce, Eu, Mn, Nd, Pr, Sm, Gd, Ib, Dy, Ho, Er, Tm, Yb, Lu, Sc, Ti, V, Cr, Fe, Co, Ni, Cu, Zn, Ir, and Pt.
It would be permissible for the light-emitting composite material 40 to comprise a combination of different inorganic crystallines 42 to obtain a color mixing result of broadband white light emission. For example, two or more UV- or violet-short wavelength inorganic crystalline materials 42 in the 350 nm to 430 nm range will absorb the first wavelength from the LED source 12 and reemit a combination of red, green, and blue light to achieve a broadband white. The broadband white resulting from a color-mixing light-emitting composite 40 is more highly uniform as compared to conventional phosphor color mixing because the emissions of red, green, and blue originate from the same location. In another example, where blue or blue-green short wavelength LED sources 12 are used (430 nm to 500 nm), these inorganic crystalline materials 42 will reemit the first wavelength in combination with red and green light to achieve a broadband white.
The glassy material 44 in which the inorganic crystalline material is suspended can include an optical glass or other glass material, such as those manufactured by Schott North America (Elmsford, N.Y.) including SF-57, SF-67, LASF-9. LASRP47, SK-57. PK-51, PK-53, FK-51A, and FK-5. Other optical glasses can include those according to the teachings of U.S. Appl. No. 2005/0075234 or U.S. Pat. No. 3,960,579, which are hereby incorporated by reference, in their entirety.
The glassy material 44 can comprise about 10% to about 99.9% of the light emitting composite material 40 by weight.
As indicated above, the selection of an inorganic crystalline 42 and glassy material 44 should be according to index-matching. That is, the index of refraction, nc, of the inorganic crystalline 42 should be approximately equal to the index of refraction, ng, of the glassy material to provide an index of refraction, nz, for the light-emitting composite material 40.
By nearly index-matching the inorganic crystalline 42 to the glassy material 44, scattering induced loss is nearly eliminated. That is, by establishing no ng that is approximately equal to nc, the phosphor-emission will travel at a speed within the inorganic crystalline 42 that is approximately equal to the travel speed within the glassy material 44 and thus reduce refraction, or a change in the direction of the emission. As a result scattering is reduced and ηp increased.
Total internal reflections occur when the interface between first and second material 52, 54 cannot be traversed by light, as illustrated with a conventional LED device 50 in
r/R≤n1/n2 Equation 3
Often, this material external to the ELIXIR LED 10 will be air, or vacuum, having n1=1. Thus, total internal reflection inside the optic 22 will be avoided when r/R is less than the inverse of n2.
The ELIXIR LED 10 of
Finally, the optic 22 positioned externally to the light-emitting composite material 40 can be constructed of a glass material similar to the glassy material 44 of the light-emitting composite material 40. Other materials can also be used so long as refractive index of the optic 22 is greater than or equal to n2. Suitable materials for the optic 22 construction can be polymethyl methacrylate (PMMA), silicones, and glasses having refractive indices of about 1.3 to about 2.2.
When PMMA is used in constructing the optic 22, the method can include polymerization of a methyl methacrylate monomer around a 25 mL round bottom flask to form an inner radius of the optic 22 with an inner diameter of approximately 3.8 cm. The outer diameter of the optic 22 can be shaped, for example, by an aluminum mold. However, other fabrication methods would be known and the size could be varied according to a particular need.
The monomer for constructing the optic 22 can be purified to eliminate contaminants. For PMMA, the methyl methacrylate monomer can be washed with a solution of sodium hydroxide, rinsed with deionized water, and dried with anhydrous magnesium sulfate. Polymerization can be initiated by benzoyl peroxide and heating the solution to 90° C. The resultant viscous solution is then poured into a mold, such as the one described previously, and then cured in an oven at 35° C. for one week.
The optic 22 could also be produced with a high quality injection molding of PMMA rather than polymerization.
While the ELIXIR LED 10 of
In other embodiments, the NIMLGCC can be used with visible diode-pumped solid-state lasers 84 as illustrated in
However, the YAG:Nd population inversion crystal 76 and KTP doubling crystal 82 are a highly expensive component of the conventional pumped solid-state laser 64. The NIMLGCC, as explained above, can provide an economical and energetically efficient alternative to the conventional pumped solid-state laser 64.
For example, as in
In yet another embodiment, the NIMLGCC can be used as a luminescence collector 90 for energy conversion, as shown in
In operation of the light tube 92, a light source 104 emits a first wavelength incident 106 to the light tube 92. The first wavelength is absorbed by an inorganic crystalline 42 within the NIMLGCC light tube 92 and reemitted at a second wavelength. This second wavelength is transmitted through the light tube 92 by total internal reflection 96 to the first or second ends 98, 100 of the light tube 92. As the second wavelength leaves the light tube 92 at the first or second ends 98, 100 as reflected light 108, the reflected light 108 impacts a photovoltaic cell 110. The photovoltaic cell 110 collects a substantial portion of the reflected light 108 and converts the reflected light 108 into another energy, such as electrical current.
The light tube 92 can be constructed with a small edge profile, which enables the use of a relatively small photovoltaic cell 110. Thus, the first and second ends 98, 100 of the light tube 92 are approximately similar in size to the surface area of the photovoltaic cell 110. This allows for increased likelihood that the reflected light 108 will impact the photovoltaic cell 110.
Suitable materials for the photovoltaic cell are known, but can generally include Si, Ge, GaAs, AlAs, InAs, AlP, InP, GaP, ZnSe, or CdSe, or combinations thereof.
The efficiency of the ELIXIR LED 10 according to the present invention is demonstrated with a computer simulation of a ray tracing diagram, shown in
The ray tracing diagram illustrates the various paths the phosphor-emitting photons can take in exiting the ELIXIR LED 10. Ray 1 exits the ELIXIR LED 10 without encountering any reflections and comprises approximately 35% of the phosphor-emissions. Ray 2 (representing approximately 35% of the phosphor-emission) demonstrates one particular benefit of the ELIXIR LED 10. Ray 2 is emitted in a direction toward the planar reflector 16, where substantial emissions loss occurs in a conventional pcLED package design. However, in the ELIXIR LED 10, the phosphor emission is reflected at the phosphor-air interface 112. Ray 2 can then exit the ELIXIR LED 10 and may avoid the planar reflector 16 entirely. Ray 3, comprising approximately 17% of the phosphor-emission, heads directly to the reflector 16 before exiting the ELIXIR LED 10 and never encounters the phosphor-air interface 112. Ray 4 is transmitted across the phosphor-air interface 112 but avoids the LED source 12 and recrosses the phosphor-air interface 112 before exiting the ELIXIR LED 10. The transmissions represented by Ray 4 account for approximately 13% of the total phosphor emissions. Finally, Ray 5 is transmitted across the phosphor-air interface 112 and enters the LED source 12 where the highest losses would occur within conventional LED package designs. In the ELIXIR LED 10 constructed with a radius of the phosphor 14, Ray 5 comprises less than 0.1% of the total phosphor-emission.
While the invention has been illustrated by a description of various embodiments and while these embodiments have been described in considerable detail, it is not the intention of the applicants to restrict or in any way limit the scope of the appended claims to such detail. Additional advantages and modifications will readily appear to those skilled in the art. Thus, the invention in its broader aspects is therefore not limited to the specific details, representative apparatus and method, and illustrative example shown and described. Accordingly, departures may be made from such details without departing from the spirit or scope of applicants' general inventive concept.
This application is a continuation application of U.S. patent application Ser. No. 15/236,127, filed Aug. 12, 2016, which is a continuation application of U.S. patent application Ser. No. 14/792,501, filed Jul. 6, 2015, which is a continuation application of U.S. patent application Ser. No. 14/444,829, filed Jul. 28, 2014, which is a continuation of U.S. patent application Ser. No. 13/794,060, filed Mar. 11, 2013, which is a continuation application of U.S. patent application Ser. No. 12/669,579, filed Jun. 28, 2010, which is a 371 of International Application PCT/US2008/070621, filed Jul. 21, 2008, which in turn, is a non-provisional application of U.S. Provisional Application No. 60/961,185, filed Jul. 19, 2007, the disclosures of which are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
3960579 | Broerner | Jun 1976 | A |
4038448 | Boyd et al. | Jul 1977 | A |
4240692 | Winston | Dec 1980 | A |
4301461 | Asano | Nov 1981 | A |
4374749 | Cusano et al. | Feb 1983 | A |
4389118 | Yuasa et al. | Jun 1983 | A |
4797609 | Yang | Jan 1989 | A |
4907044 | Schellhorn et al. | Mar 1990 | A |
5001609 | Gardner et al. | Mar 1991 | A |
5055892 | Gardner et al. | Oct 1991 | A |
5268635 | Bortolini et al. | Dec 1993 | A |
5282088 | Davidson | Jan 1994 | A |
5331393 | Hopkins | Jul 1994 | A |
5335152 | Winston | Aug 1994 | A |
5424855 | Nakamura et al. | Jun 1995 | A |
5727108 | Hed | Mar 1998 | A |
5856727 | Schroeder et al. | Jan 1999 | A |
6066861 | Hohn | May 2000 | A |
6095655 | Bigliati et al. | Aug 2000 | A |
6111367 | Asano et al. | Aug 2000 | A |
6155699 | Miller et al. | Dec 2000 | A |
6236331 | Dussureault | May 2001 | B1 |
6479942 | Kimura | Nov 2002 | B2 |
6495964 | Muthu et al. | Dec 2002 | B1 |
6527411 | Sayers | Mar 2003 | B1 |
6617560 | Forke | Sep 2003 | B2 |
6642618 | Yagi et al. | Nov 2003 | B2 |
6819505 | Cassarly et al. | Nov 2004 | B1 |
7015514 | Baur et al. | Mar 2006 | B2 |
7091653 | Ouderkirk et al. | Aug 2006 | B2 |
7151283 | Reeh et al. | Dec 2006 | B2 |
7286296 | Chaves et al. | Oct 2007 | B2 |
7306960 | Bogner et al. | Dec 2007 | B2 |
7329907 | Pang | Feb 2008 | B2 |
7329998 | Jungwirth | Feb 2008 | B2 |
7344902 | Basin et al. | Mar 2008 | B2 |
7355284 | Negley | Apr 2008 | B2 |
7514867 | Yano et al. | Apr 2009 | B2 |
7522802 | Shiau et al. | Apr 2009 | B2 |
7828453 | Tran et al. | Nov 2010 | B2 |
7859190 | Shi | Dec 2010 | B2 |
7889421 | Narendran et al. | Feb 2011 | B2 |
8007118 | O'Neill et al. | Aug 2011 | B2 |
8083364 | Allen | Dec 2011 | B2 |
8168998 | David et al. | May 2012 | B2 |
8314537 | Gielen et al. | Nov 2012 | B2 |
8362695 | Aanegola et al. | Jan 2013 | B2 |
8436380 | Aanegola et al. | May 2013 | B2 |
8598778 | Allen et al. | Dec 2013 | B2 |
8791631 | Allen et al. | Jul 2014 | B2 |
9078332 | Allen | Jul 2015 | B2 |
9441818 | Dixon et al. | Sep 2016 | B2 |
9482396 | Dixon et al. | Nov 2016 | B2 |
9494293 | Pickard | Nov 2016 | B2 |
9683710 | Schinagl | Jun 2017 | B2 |
9822951 | Lu et al. | Nov 2017 | B2 |
10107475 | Smith et al. | Oct 2018 | B2 |
20030117087 | Barth et al. | Jun 2003 | A1 |
20030235050 | West et al. | Dec 2003 | A1 |
20040051111 | Ota | Mar 2004 | A1 |
20040052076 | Mueller et al. | Mar 2004 | A1 |
20040120155 | Suenaga | Jun 2004 | A1 |
20040150991 | Ouderkirk et al. | Aug 2004 | A1 |
20040223315 | Suehiro et al. | Nov 2004 | A1 |
20050023545 | Camras et al. | Feb 2005 | A1 |
20050075234 | Wolff et al. | Apr 2005 | A1 |
20050127833 | Tieszen | Jun 2005 | A1 |
20050185416 | Lee et al. | Aug 2005 | A1 |
20050243570 | Chaves et al. | Nov 2005 | A1 |
20050269582 | Mueller et al. | Dec 2005 | A1 |
20060097245 | Aanegola et al. | May 2006 | A1 |
20060126343 | Hsieh et al. | Jun 2006 | A1 |
20060152140 | Brandes | Jul 2006 | A1 |
20060152931 | Holman | Jul 2006 | A1 |
20060255353 | Taskar et al. | Nov 2006 | A1 |
20070018102 | Braune et al. | Jan 2007 | A1 |
20070081336 | Bierhuizen et al. | Apr 2007 | A1 |
20070170447 | Negley | Jul 2007 | A1 |
20070256453 | Barnes et al. | Nov 2007 | A1 |
20070257267 | Leatherdale et al. | Nov 2007 | A1 |
20070273282 | Radkov et al. | Nov 2007 | A1 |
20080054280 | Reginelli et al. | Mar 2008 | A1 |
20080079910 | Rutherford et al. | Apr 2008 | A1 |
20080080166 | Duong et al. | Apr 2008 | A1 |
20080101754 | Parker et al. | May 2008 | A1 |
20080112183 | Negley | May 2008 | A1 |
20080297027 | Miller et al. | Dec 2008 | A1 |
20090008662 | Ashdown | Jan 2009 | A1 |
20090050919 | Weijers et al. | Feb 2009 | A1 |
20090200939 | Lenk et al. | Aug 2009 | A1 |
20090201677 | Hoelen et al. | Aug 2009 | A1 |
20090272996 | Chakraborty | Nov 2009 | A1 |
20090296407 | Bailey | Dec 2009 | A1 |
20090310352 | Chang | Dec 2009 | A1 |
20100066236 | Xu et al. | Mar 2010 | A1 |
20100073927 | Lewin et al. | Mar 2010 | A1 |
20100097821 | Huang et al. | Apr 2010 | A1 |
20100123386 | Chen | May 2010 | A1 |
20100134016 | York et al. | Jun 2010 | A1 |
20100148151 | Camras et al. | Jun 2010 | A1 |
20100172120 | Wegh et al. | Jul 2010 | A1 |
20100232134 | Tran | Sep 2010 | A1 |
20100263723 | Allen et al. | Oct 2010 | A1 |
20100264432 | Liu et al. | Oct 2010 | A1 |
20100290226 | Harbers et al. | Nov 2010 | A1 |
20100301367 | Nakamura et al. | Dec 2010 | A1 |
20100301727 | Lenk et al. | Dec 2010 | A1 |
20100308354 | David et al. | Dec 2010 | A1 |
20110080108 | Chiang et al. | Apr 2011 | A1 |
20110089817 | Lyons et al. | Apr 2011 | A1 |
20110176091 | Boonekamp et al. | Jul 2011 | A1 |
20110182065 | Negley et al. | Jul 2011 | A1 |
20110227037 | Su | Sep 2011 | A1 |
20110267800 | Tong et al. | Nov 2011 | A1 |
20110267801 | Tong et al. | Nov 2011 | A1 |
20110273882 | Pickard | Nov 2011 | A1 |
20110291130 | Diana et al. | Dec 2011 | A1 |
20110298371 | Brandes et al. | Dec 2011 | A1 |
20120033403 | Lamvik et al. | Feb 2012 | A1 |
20120039073 | Tong | Feb 2012 | A1 |
20120068205 | Galvez et al. | Mar 2012 | A1 |
20120112219 | Jang et al. | May 2012 | A1 |
20120112661 | Van de Ven et al. | May 2012 | A1 |
20120119221 | Negley | May 2012 | A1 |
20120127694 | Richardson | May 2012 | A1 |
20120140436 | Yang et al. | Jun 2012 | A1 |
20120147296 | Montgomery et al. | Jun 2012 | A1 |
20120181565 | David et al. | Jul 2012 | A1 |
20120187441 | Li | Jul 2012 | A1 |
20120287602 | Urano | Nov 2012 | A1 |
20120327656 | Ramer et al. | Dec 2012 | A1 |
20130021776 | Veerasamy et al. | Jan 2013 | A1 |
20130201715 | Dau et al. | Aug 2013 | A1 |
20140333198 | Allen et al. | Nov 2014 | A1 |
20150241029 | York | Aug 2015 | A1 |
Number | Date | Country |
---|---|---|
101832529 | Sep 2010 | CN |
2006-352030 | Dec 2006 | JP |
2007-49019 | Feb 2007 | JP |
2007053366 | Mar 2007 | JP |
2007157686 | Jun 2007 | JP |
2009-177095 | Aug 2009 | JP |
2010206085 | Sep 2010 | JP |
2009510764 | Jan 2012 | JP |
WO0107828 | Feb 2001 | WO |
WO 0127962 | Apr 2001 | WO |
WO03017729 | Feb 2003 | WO |
WO04076916 | Sep 2004 | WO |
WO2007037662 | Apr 2007 | WO |
WO2007081812 | Jul 2007 | WO |
2009145298 | Dec 2009 | WO |
2010067292 | Jun 2010 | WO |
PCTIB2011052874 | Jun 2011 | WO |
WO2011112914 | Sep 2011 | WO |
WO 2013078463 | May 2013 | WO |
Entry |
---|
Allen, et al. “A nearly ideal phosphor-converted white light-emitting diode”, Applied Physics Letters, vol. 92 (2008) 3 pages. |
Allen, et al. “ELiXIR—Solid-State Luminaire With Enhanced Light Extraction by Internal Reflection”, Journal of Display Technology, vol. 3, No. 2, Jun. 2007 pp. 155-159. |
Allen, et al., “Highly Efficient light-emitting composite material for solid-state illumination devices, lasers, and luminescent collectors”, U.S. Appl. No. 60/961,185, filed Jul. 19, 2007, 38 pages. |
Carclo Technical Plastics “Luxeon® I 20 & 26.5mm Range”, downloaded from the internet at: http://docs-europe.electrocomponents.com/webdocs/0dcb/0900766b80dcbbeb.pdf on Oct. 30, 2012, 31 pages. |
Intematix, “Design Considerations for ChromaLit™ Ellipse, Candle, and Dome Remote Phosphor Light Sources”, Jan. 11, 2012, downloaded from the internet at: http://www.intematix.com/uploads/files/imx-design-consideratious-ecd-app-note.pdf, on Oct. 30, 2012, 23 pages. |
Intematix, “Mixing Chamber Design Considerations for ChromaLit™ Remote Phosphor Light Sources”, Aug. 29, 2012, downloaded from the internet at: http://www.intematix.com/uploads/files/intematix_mixing_chamber_design_for_chormalit.pdf on Oct. 30, 2012, 12 pages. |
International Bureau of WIPO, International Preliminary Report on Patentability, PCT/US2008/070621, dated Jan. 19, 2010, 6 pages. |
International Searching Authority, The International Search Report and Written Opinion of the International Searching Authority, PCT/US2008/070621, dated Sep. 26, 2008, 9 pages. |
International Searching Authority, The International Search Report and Written Opinion of the International Searching Authority, PCT/US2012/66463, dated Apr. 2, 2013, 18 pages. |
Liu, et al. “Effects of Phosphor's Location on LED Packaging Performance”, 2008 International Conference on Electronic Packaging Technology & High Density Packaging (ICEPT-HDP 2008), 7 pages. |
Liu, et al. “Effects of Phosphor's Thickness and Concentration on Performance of White LEDs”, 2008 International Conference on Electronic Packaging Technology & High Density Packaging (ICEPT-HDP 2008), 6 pages. |
Mims III, Forrest, “Sun Photometer with Light-Emitting Diodes as Spectrally Selective Detectors”, Applied Optics 31, 6965-6967, 1992. |
Carr et al., “One-Watt GaAs p-n Junction Infrared Source”, Applied Physics Letters, vol. 3, No. 10, Nov. 15, 1963, pp. 173-175. |
W. N. Carr, “Photometric Figures of Merit for Semiconductor Luminescent Sources Operating in Spontaneous Mode”, Infrared Physics, 1966, vol. 6, pp. 1-19. |
Authorized Officer Blaine R. Copenheaver, Notification of Transmittal of the International Search Report and Written Opinion, International Application No. PCT/US2013/059511, dated Feb. 14, 2014, 7 pages. |
Authorized Officer Blaine R. Copenheaver, Notification of Transmittal of the International Search Report and Written Opinion, International Application No. PCT/US2013/059545, dated Feb. 14, 2014, 15 pages. |
Authorized Officer Blaine R. Copenheaver, Notification of Transmittal of the International Search Report and Written Opinion, International Application No. PCT/US2013/059544, dated Feb. 14, 2014, 9 pages. |
Authorized Officer Blaine R. Copenheaver, Notification of Transmittal of the International Search Report and Written Opinion, International Application No. PCT/US2013/059525, dated Feb. 19, 2014, 9 pages. |
Authorized Officer Blaine R. Copenheaver, Notification of Transmittal of the International Search Report and Written Opinion, International Application No. PCT/US2014/021778, dated Jun. 23, 2014, 11 pages. |
Japanese Application No. 2014-543597, Decision of Rejection, dated Apr. 24, 2017, 130 pages. |
Number | Date | Country | |
---|---|---|---|
20190101261 A1 | Apr 2019 | US |
Number | Date | Country | |
---|---|---|---|
60961185 | Jul 2007 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 15236127 | Aug 2016 | US |
Child | 15965793 | US | |
Parent | 14792501 | Jul 2015 | US |
Child | 15236127 | US | |
Parent | 14444829 | Jul 2014 | US |
Child | 14792501 | US | |
Parent | 13794060 | Mar 2013 | US |
Child | 14444829 | US | |
Parent | 12669579 | US | |
Child | 13794060 | US |