The disclosure relates to the field of LED illumination and more particularly to techniques for producing arrays of violet LEDs coated with densely-packed-luminescent-material layers.
Legacy implementations of white LED light sources have been constructed by encircling an array of blue LED die with a reflective white dam and filling the area inside the dam with a silicone-phosphor mix. This legacy approach results in the blue LED die being surrounded by luminescent-materials-containing silicone, yet the resulting legacy implementations exhibit several significant drawbacks. First, light emitted by the luminescent materials that are located far from the LED die is scattered many times before being able to exit the structure. In the process of doing so, this light can be absorbed by other luminescent-material particles, adjacent LED die (if any), and/or by the materials that form the base of the structure (i.e., submount materials). While the reflectivity of the submount materials have been specially treated, for example, by coating the submount surface with either a high-reflectivity white coating or with highly-reflective metals such as silver, some fraction of the light is converted to heat, and the efficiency of light emission is reduced. A more desirable optical configuration is to fabricate such light sources with luminescent-materials particles juxtaposed in a spatial region very near the LED die themselves. In this manner, light scattering by luminescent-material particles far from the die and absorption by the submount materials can be reduced, and the efficiency of such a light source can be improved. For example, to conformally coat the die with a phosphor material a laminar sheet of silicone or other binder, which is impregnated with phosphors, is hot-rolled onto the LED die. This method has the disadvantage that there is poor coverage on the sides of the LED die, which result in reduced light output.
However, in order to have the luminescent materials particles confined to a spatial region very near the LED die themselves, what is needed is an inexpensive method of applying one or more conformal layers (e.g., coatings) of luminescent materials around LED die in order to improve the light emission efficiency of the LED light source while concurrently providing for desired color balance as well as reliable operation under high current density operation.
To improve the light emission efficiency of an LED light source a high-aspect ratio photoresist is used to create cavities that are then filled with phosphors. The methods provide devices in which the phosphor covers the sides of the LED die.
In a first aspect, methods for coating violet-emitting LED die with densely-packed-luminescent-materials are provided, comprising attaching an arrangement of a one or more violet-emitting LED die to a submount structure; applying a photoresist characterized by a thickness greater than a height of at least some of the one or more violet-emitting LED die; opening a first cavity hole in the photoresist around at least some of the one or more violet-emitting LED die; dispensing a luminescent material into the first cavity hole; and stripping the photoresist to provide one or more densely-packed-luminescent-materials coated violet-emitting LED die.
In a second aspect, apparatus are provided, comprising a submount; a violet-emitting LED die attached to the submount, wherein the perimeter of the die forms an area; and
a coating covering at least one surface of the violet-emitting LED die, wherein the coating comprises at least one luminescent material.
In a third aspect, apparatus are provided, comprising a lamp base; a submount; a violet-emitting LED die attached to the submount and electrically connected to the lamp base, wherein the perimeter of the violet-emitting LED die forms a triangular area; and a coating covering at least one surface of the violet-emitting LED die, wherein the coating comprises at least one luminescent material.
Those skilled in the art will understand that the drawings, described herein, are for illustration purposes only. The drawings are not intended to limit the scope of the present disclosure.
FIG. 13F1 and FIG. 13F2 characterize the dimensions given as N, S, E, and W, and Top which dimensions are used to define the phosphor layer thickness around the LED die according to some embodiments.
FIG. 13G1 and FIG. 13G2 show charts for comparisons of color variation from phosphor layer asymmetries. The variations are many times smaller for a violet-based LED as compared to a blue-based LED.
FIGS. 16A1 through
The term “exemplary” is used herein to mean serving as an example, instance, or illustration. Any aspect or design described herein as “exemplary” is not necessarily to be construed as preferred or advantageous over other aspects or designs. Rather, use of the word exemplary is intended to present concepts in a concrete fashion.
The term “or” is intended to mean an inclusive “or” rather than an exclusive “or”. That is, unless specified otherwise, or is clear from the context, “X employs A or B” is intended to mean any of the natural inclusive permutations. That is, if X employs A, X employs B, or X employs both A and B, then “X employs A or B” is satisfied under any of the foregoing instances. In addition, the articles “a” and “an” as used in this application and the appended claims should generally be construed to mean “one or more” unless specified otherwise or is clear from the context to be directed to a singular form.
Reference is now made in detail to certain embodiments. The disclosed embodiments are not intended to be limiting of the claims.
The compositions of wavelength-converting materials referred to in the present disclosure comprise various luminescent materials. And, the compositions of luminescent materials referred to in the present disclosure comprise various wavelength-converting materials.
Wavelength-conversion materials can be ceramic or semiconductor particle phosphors, ceramic or semiconductor plate phosphors, organic or inorganic downconverters, upconverters (anti-stokes), nano-particles and other materials which provide wavelength conversion. Some examples are listed below:
(Srn,Ca1−n)10(PO4)6*B2O3:Eu2+ (wherein 0≦n≦1)
(Ba,Sr,Ca)5(PO4)3(Cl,F,Br,OH):Eu2+,Mn2+
(Ba,Sr,Ca)BPO5:Eu2+,Mn2+
Sr2Si3O8*2SrC12:Eu2+
(Ca,Sr,Ba)3MgSi2O8:Eu2+, Mn2+
BaAl8O13:Eu2+
2SrO*0.84P2O5*0.16B2O3:Eu2+
(Ba,Sr,Ca)MgAl10O17:Eu2+,Mn2+
K2SiF6:Mn4+
(Ba,Sr,Ca)Al2O4:Eu2+
(Y,Gd,Lu,Sc,La)BO3:Ce3+,Tb3+
(Ba,Sr,Ca)2(Mg,Zn)Si2O7:Eu2+
(Mg,Ca,Sr,Ba,Zn)2Si1−xO4−2x:Eu2+ (wherein 0≦x≦0.2)
(Ca, Sr, Ba)MgSi2O6:Eu2+
(Sr,Ca,Ba)(Al,Ga)2S4:Eu2+
(Ca, Sr)8(Mg,Zn)(SiO4)4C12:Eu2+,Mn2+
Na2Gd2B2O7:Ce3+,Tb3+
(Sr,Ca,Ba,Mg,Zn)2P2O7:Eu2+,Mn2+
(Gd,Y,Lu,La)2O3:Eu3+,Bi3+
(Gd,Y,Lu,La)2O2S:Eu3+,Bi3+
(Gd,Y,Lu,La)VO4:Eu3+,Bi3+
(Ca,Sr)S:Eu2+,Ce3+
(Y,Gd,Tb,La,Sm,Pr,Lu)3(Sc,Al,Ga)5−nO12−3/2n:Ce3+ (wherein 0≦n≦0.5)
ZnS:Cu+,Cl−
(Y,Lu,Th)3Al5O12:Ce3+
ZnS:Cu+,Al3+
ZnS:Ag+,Al3+
ZnS:Ag+,Cl−
Ca1−xAlx−xySi1−x+xyN2−x−xyCxy:A
Ca1−x−zNazM(III)x−xy−zSi1−x+xy+zN2−x−xyCxy:A
M(II)1−x−zM(I)zM(III)x−xy−zSi1−x+xy+zN2−x−xyCxy:A
M(II)1−x−zM(I)zM(III)x−xy−zSi1−x+xy+zN2−x−xy−2w/3CxyOw−v/2Hv:A
M(II)1−x−zM(I)zM(III)x−xy−zSi1−x+xy+zN2−x−xy−2w/3−v/3CxyOwHv:A
wherein 0<x<1, 0<y<1, 0≦z<1, 0≦v<1, 0<w<1, x+z<1, x>xy+z, and 0<x−xy−z<1, M(II) is at least one divalent cation, M(I) is at least one monovalent cation, M(III) is at least one trivalent cation, H is at least one monovalent anion, and A is a luminescence activator doped in the crystal structure.
LaAl(Si6−zAlz)(N10−zOz):Ce3+ (wherein z=1)
(Ca, Sr) Ga2S4:Eu2+
AlN:Eu2+
SrY2S4:Eu2+
CaLa2S4:Ce3+
(Ba,Sr,Ca)MgP2O7:Eu2+,Mn2+
(Y,Lu)2WO6:Eu3+,Mo6+
CaWO4
(Y,Gd,La)2O2S:Eu3+
(Y,Gd,La)2O3:Eu3+
(Ba,Sr,Ca)nSinNn:Eu2+ (where 2n+4=3n)
Ca3(SiO4)Cl2:Eu2+
(Y,Lu,Gd)2−nCanSi4N6+nC1−n:Ce3+, (wherein 0≦n≦0.5)
(Lu,Ca,Li,Mg,Y) alpha-SiAlON doped with Eu2+ and/or Ce3+
(Ca,Sr,Ba)SiO2N2:Eu2+,Ce3+
Ba3MgSi2O8:Eu2+,Mn2+
(Sr,Ca)AlSiN3:Eu2+
CaAlSi(ON)3:Eu2+
Ba3MgSi2O8:Eu2+
LaSi3N5:Ce3+
Sr10(PO4)6Cl2:Eu2+
(BaSi)O12N2:Eu2+
M(II)aSibOcNdCe:A wherein (6<a<8, 8<b<14, 13<c<17, 5<d<9, 0<e<2) and M(II) is a divalent cation of (Be,Mg,Ca,Sr,Ba,Cu,Co,Ni,Pd,Tm,Cd) and A of (Ce,Pr,Nd,Sm,Eu,Gd,Tb,Dy,Ho,Er,Tm,Yb,Lu,Mn,Bi,Sb)
SrSi2(O,Cl)2N2:Eu2+
SrSi9Al19ON31:Eu2+
(Ba,Sr)Si2(O,Cl)2N2:Eu2+
LiM2O8:Eu3+ where M=(W or Mo).
For purposes of the application, it is understood that when a luminescent material has two or more dopant ions (i.e., those ions following the colon in the above luminescent materials), this is to mean that the luminescent material has at least one (but not necessarily all) of those dopant ions within the material. That is, as understood by those skilled in the art, this type of notation means that the luminescent material can include any or all of those specified ions as dopants in the formulation.
Further, it is to be understood that nanoparticles, quantum dots, semiconductor particles, and other types of materials can be used as wavelength-converting materials. The list above is representative and should not be taken to include all the materials that may be utilized within embodiments described herein.
Improvements to be addressed include high-current-density/high-power LED applications where luminescent-material-particle heating can reduce efficiency and reduce lifetime. The LED die in such applications emit a large flux of photons, which, when absorbed by the luminescent-material particles that surround the LED die, generate substantial heat in the luminescent material particles as a result of the photon down-conversion process. Often this down-conversion-generated heat accumulates in the luminescent-material particles due to the poor thermal conductivity of the silicone in which they are dispersed. One result of the accumulated heat is a significant temperature rise in the luminescent-material particles. This temperature rise has the effects of reducing the photon down-conversion efficiency as well as causing decomposition (e.g., browning or cracking) of the surrounding silicone encapsulant. One solution to this problem is to have the luminescent materials packed so tightly around the LED die that they maintain thermal contact both with each other, with the submount, and with the LED die surface. In this configuration, heat can then be efficiently transported from the luminescent materials particles through the submount and LED die themselves and out the back of the package (e.g., in the case that the thermal conductivity of both the luminescent-material particles and the LED die are higher those of silicone encapsulants).
Legacy techniques provide for deposition of layers on the surface of an LED wafer which can later be diced into individual LED die, however, this coating process is inappropriate for three-dimensional LED die. What is disclosed herein is an approach to coating three-dimensional violet LED die with a dense layer of luminescent-material particles.
One approach is to conformally coat the LED die using an electrophoretic-deposition (EPD) process. However, a precisely-controlled luminescent-material-deposition process is required when blue-emitting LED die are employed as the amount of blue leakage into the final white spectrum needs to be ultra-precisely controlled. EPD deposition systems are complex and, as a result, this coating process is expensive—particularly if multi-layer coatings are desired. By employing violet-emitting LED die instead of blue-emitting LED die, the need for such ultra-precise luminescent-material-thickness control is reduced—enabling the use of less-complex luminescent-material deposition processes. In some cases employing a dense-luminescent-material layer provides thermal control based at least in part on the characteristics of the selected luminescent-material(s). When the density of the luminescent materials in the coating is insufficient to allow reasonable thermal contact between them, thermally-conductive and optically-transparent materials can be added to the coating to improve the overall thermal conductivity of the layer. Exemplary thermally-conductive and optically-transparent materials are listed in Table 1.
In addition to the examples of Table 1, other materials can be used such as, for example, Zinc Fluoride—ZnF2, Iron Fluoride—FeF2, Cerium Fluoride—CeF3, Potassium Dihydrogen Phosphate—KH2PO4, Aluminum phosphate—AlPO4, and Potassium sulfate (K2SO4).
Further, there are a number of groups of materials (e.g., complex fluorides such as KMeF3, phosphates, and sulfates) having characteristics within the desired ranges.
Now, referring to the aforementioned
1) Attach violet LED die 210 (e.g., flip-chip LED die) to a submount 220 structure (e.g., a silicon or ceramic submount).
2) Apply resist layer (e.g., a thick-film) to the LED die array. As shown, the resist layer thickness is slightly larger than the height of the LED die. In this configuration, the height of the resist can substantially influence the final thickness of the luminescent materials coating on the top surface of the die. The thickness of the luminescent materials coating on the top of the die can thus be independently adjusted relative to the thickness of the luminescent-materials coating on the sides of the die. The thickness of the luminescent materials coating on the sides of the die can be controlled by the size of the openings in the resist layer.
3) Open holes in the resist around the LED die using photolithography. Non-flip chip designs may also provide for opening holes in the resist around the wirebond pads.
4) Wirebond the die as needed (e.g., if they are not of a flip-chip configuration).
5) Dispense a dense layer of luminescent materials into the cavities (e.g., cavity 240) that surround the LED die and on top of the LED die. This dense layer can be comprised of a powder layer of luminescent materials or a combination of luminescent materials and transparent, thermally-conductive particles (see Table 1). Alternatively, the luminescent materials can be dispensed in a solvent solution, which is then allowed to evaporate away—leaving a dense-luminescent-material layer, or, the luminescent materials can be dispensed directly in a very-heavily-loaded-silicone mixture.
6) Fix the luminescent materials around the LED die by depositing (e.g., using a dispense needle 270) a silicone (e.g., silicone 250), sol gel, or other stable binding material to the luminescent materials (if they were not dispensed already pre-mixed in a silicone).
7) Strip the thick film (or other) resist material with, for example, an O2 plasma-etch system. A photoresist is selected to have a low etch rate of the binding material so as to enable the resist to be selectively removed—leaving behind the luminescent-materials-coating layer that surrounds each LED die. The etch rate of the binding material should thus be, for example >10× less than that of the photoresist 230.
8) Some embodiments (e.g., see
9) Some embodiments place a reflective dam around a set of die on the submount and fill the dam with either clear silicone 310 or silicone loaded with a small amount of diffusant (e.g., to improve light-source uniformity).
10) Dice the silicon or ceramic submount into individual light sources.
11) Some embodiments affix a large lens to the reflective dam (if employed) to further improve light-extraction efficiency.
The result of performing the foregoing steps is a light source apparatus in the form of a two-dimensional arrangement of violet LED die that have been coated with a dense, luminescent material layer. Other embodiments (see
As shown, a dam is placed around the LED die array and the dam is filled with a phosphor-loaded silicone.
As shown in
In some embodiments, the following steps are taken:
As shown, the dam forms a moat around the LED die and defines the outer shape of the luminescent-material layer, and the dam that surrounds LED die is made of a material that is transparent to visible light (e.g., clear silicone). The dam, in such embodiments, acts as an encapsulant for the sides of the linear light source. In addition, the dam forms a clear base upon which a clear silicone lens cap can be dispensed (see
The aforementioned techniques for fabricating arrays of violet LED die coated with densely-packed-luminescent-material layers include depositing a layer over an array of die. Other techniques serve to coat individual LED die. In particular, the embodiments disclosed below pertain to a method for fabricating luminescent-material-coated individual LED die using photolithography processes. The disclosed methods include techniques where luminescent materials can be applied onto individual LED die in a manner that removes or reduces the need for a dam. Also, the photolithography processes can be tuned to vary the thickness of luminescent-materials on the top or sides of individual single- or multi-LED-die array. Tuning can be done in accordance with light output requirements. In some cases, luminescent materials are applied onto individual LED die after wire-bonds have been formed. Further, certain techniques in which luminescent materials are applied onto individual LED die serve to lower luminescent-material back scattering (e.g., resulting in a higher efficiency). Still further, certain techniques in which luminescent materials are applied result in higher luminescent material loading, which in turn can result in a decrease in operating temperatures (e.g., allowing integration of high index silicone in the luminescent material mix).
The aforementioned techniques and properties open up the possibility to:
As discussed herein and below, luminescent-material-coated individual LED die are formed using photolithography. Strictly as examples, the process can proceed as follows:
Some embodiments include two layers of luminescent material coating the die. In one particular processing flow, certain spin steps are carried out at lower spin speeds (e.g., spins at 300 rpm for 20 s, 900 rpm for 3.5 s, 400 rpm 14 s). For multi-layer luminescent-material combinations, a second layer of photoresist is spun such that it is slightly thicker (e.g., about 0.5 μm thicker) than the first layer so as to barely cover the luminescent material patterned during processing of the first layer.
Several possible techniques to fabricate luminescent-material-coated LED die using photolithography processes is described in
The subassembly 10A00 is subjected to a photoresist spin-on process to form subassembly 10B00. Then a mask and photoresist process is used to form subassembly 10000. A first layer of luminescent material is deposited (e.g., dispensed) into the recesses formed after washing away the photoresist to form subassembly 10D00, which is in turn subjected to an additional wash to form subassembly 10E00. Yet another series of photoresist, exposure, and wash steps serve to form subassembly 10F00 (apply photoresist), and subassembly 10G00 (subsequent to wash after using mask 2). A second layer of luminescent material is deposited (e.g., dispensed) into the recesses formed after forming subassembly 10G00, which subassembly 1H00 is in turn subjected to an additional washes to form subassembly 10100, having two coats of luminescent material applied to a single LED die. Additional steps with additional masks can be used to add a third or n-th layer of luminescent material.
The subassembly 11A00 is subjected to a photoresist spin-on process to form subassembly 11B00. Then a mask and photoresist process is used to form subassembly 11C00, where a first LED die is exposed. A first layer of luminescent material is deposited (e.g., dispensed) into the recesses formed after washing away the photoresist to form subassembly 11D00, which is in turn subjected to an additional wash to form subassembly 11E00. Yet another series of photoresist, exposure, and wash steps serve to form subassembly 11F00 (e.g., via application of photoresist), and subassembly 11G00 (subsequent to wash after using mask 2). A layer of second luminescent material is deposited (e.g., dispensed) over the second LED die (e.g., into the recesses formed after forming subassembly 11G00), which subassembly 1H00 is in turn subjected to an additional washes to form subassembly 11100, having different coats of luminescent material applied to first and second LED die (e.g., adjacent die, as shown). Using this technique, different luminescent materials in different thicknesses of conformal coatings can be applied to different (e.g., adjacent) LED die.
One possible way to measure the results of spectrum engineering (e.g., and to assess quality of emitted light) is to characterize the gamut of the light source. The experimental set-up considers up to 15 reflectance samples (e.g., taken from of the Color Quality Scale [Davis10]), and choosing which sample measurements are taken. From a series of measurements, chromaticity can be derived or calculated, from which in turn a gamut of resulting points can be plotted.
Also shown in
FIGS. 13F1 and 13F2 characterize the dimensions given as N, S, E, and W, and Top which dimensions are used to define the phosphor layer thickness around the LED die. Some of the figures herein present side views, corresponding to a view from a N, S, E, or W viewing orientation.
FIG. 13G1 and FIG. 13G2 show charts for comparisons of color variation from phosphor layer asymmetries. The variations are many times smaller for a violet based LED as compared to a blue based LED. Coating over the faces of the violet-emitting LED are exemplified as in the following table. Colorpoint variations corresponding to the thicknesses as shown in the following table are presented in FIG. 13G2.
The following examples describe in detail examples of constituent elements of the herein-disclosed embodiments. It will be apparent to those skilled in the art that many modifications, both to materials and methods, may be practiced without departing from the scope of the disclosure.
Example 1 follows aspects of the foregoing approach to making individual white-die arrays described above. This approach applies to fabrication using bulk-GaN-substrate-based LEDs with violet emission, and used in a high-current-density regime. Some embodiments include such white-die arrays built with violet LED die grown on bulk-GaN and some embodiments include individual violet LED die driven at high current densities (e.g., over 150 Amps/cm2 or over 175 Amps/cm2, etc.).
The apparatus formed by the techniques of Example 1, further comprising single-color red, green, and blue luminescent materials deposited around each violet LED die to reduce the light absorption that is present in mixed-luminescent-material white light sources. This can have the effect of increasing the 1 m/W efficiency of such sources. A mixture of red, green, blue, and white (RGBW) coated violet LED die could also be produced which can help with color mixing.
The apparatus formed by the techniques of Example 1, formed by depositing single-color luminescent materials around the individual violet LED die in an array. Accordingly, a bright, single-color light source can be produced.
The apparatus formed by the techniques of Example 1, further comprising depositing a multi-layer luminescent-material stack by repeating the process described herein (see
The apparatus formed by the techniques of Example 1, further comprising depositing the luminescent materials in a color-separated-layer structure around the die. For example, depositing a red luminescent-material layer prior to blue and green luminescent material layer may reduce light-absorption in the violet LED die as less of the more-likely-to-be-absorbed short-wavelength light will be scattered back into the violet LED die. The alignment precision achievable with standard photolithography techniques is more than adequate to create layered structures around each die. Strictly as an example, the first layer deposited is formed to be wide enough to account for variations in die-to-die placement on the submount; however, subsequent luminescent material layer(s) could be fairly thin.
The apparatus formed by the techniques of Example 1, further comprising a two-layer luminescent-material stack made by “dusting” the original openings in the resist layer with a desired first-to-be-deposited luminescent-material and then filling the cavities with additional luminescent materials as described above.
The apparatus formed by the techniques of Example 1, further comprising warm-white and cool-white luminescent-materials-deposited around different individually-addressable die to create color-point-tunable light sources. In some variations, different individual ones of the violet LED die have cool-white, warm-white, red, green, or blue luminescent-material coatings that are selected in a particular proportion in order to make a color-tunable-white-light source.
The apparatus formed by the techniques of Example 1, further comprising repeating for die-level encapsulation. In this case, thick-film resist can be applied, holes opened to create the appropriate side-wall shape around the luminescent-material-coated die, and clear silicone dispensed around and on-top-of each coated violet LED die in the array (see
The apparatus formed by the techniques of Example 1, including vias formed in the submount for back-side electrical connections. Using this technique facilitates making single-die white LEDs by dicing the submount into individually-coated, slightly-larger-than-die-size pieces. A lamp formed of such die exhibits the light output, and the color consistency of a violet-pumped-three luminescent-material white light source. A lamp formed of such die could exhibit high light output at the high operating temperatures desired for automotive daytime-running-lamp applications.
The apparatus formed by the techniques of Example 1, arranged into linear strips (e.g., rectangular-shaped strips) of individual die, which can be employed as tungsten-filament-like light sources. In a dipped, clear-silicone-cap version, there might be no need for further encapsulation for use as an A-lamp filament-like light source. Such linear strips may have sufficient surface brightness to now be employed in automotive-forward-lighting applications. Such linear strips can comprise a linear array of triangular-shaped violet LEDs atop a rectangular-shaped submount (or atop a rectangular-shaped area of a submount), were the violet LED die are arranged with one side of the triangular LED die facing the narrow side of the submount.
A process for fabricating violet LED die coated with densely-packed-luminescent-material layers, comprising:
The process of Example 11, wherein the violet LEDs are grown on a bulk-GaN substrate.
The process of Example 11, wherein after the dispensing of a layer of luminescent material, the opening of cavity holes is repeated with cavity holes that are larger than those of the previous layer to deposit successive separate-color-light-emitting layers.
The process of Example 11, wherein a height of the resist layer above the LED die is different than the distance from an edge of the violet LED die to a photoresist cavity wall.
The process of Example 11, wherein dispensing a layer of luminescent material comprises dispensing a blue luminescent material around certain of the violet LED die, dispensing a green luminescent material around certain of the violet LED die, and dispensing a red luminescent material around certain of the violet LED die.
The process of Example 15, wherein different ones of the violet LED die are configured to be driven independently to create a color-tunable light source.
The process of Example 11, wherein dispensing a layer of luminescent material comprises dispensing a cool-white or a warm-white luminescent material around certain of the violet LED die and the different ones of the violet LED die are configured to be driven independently to create a color-temperature-tunable light source.
The process of Example 11, wherein dispensing a layer of luminescent material comprises dispensing cool-white luminescent material, warm-white luminescent material, red luminescent material, green luminescent material, or blue luminescent material around certain of the LED die in a selected proportion to make a color-tunable-white-light source.
The process of Example 11, wherein the luminescent materials are deposited in a linear strip around a linear arrangement of violet LED die.
The process of Example 11, wherein the cavity holes comprise linear strips around linearly arranged violet LED die.
The process of Example 11, wherein the violet LEDs are triangular-shaped and the violet LEDs are arranged in a linear array with one side of the triangular violet LED facing a narrow side of the submount.
The process of Example 11, wherein the violet LEDs are triangular-shaped and the violet LEDs are arranged in a dual strip of violet LEDs having one side of the triangular-shaped violet LEDs facing a wide side of the submount.
The process of Example 11, further comprising encapsulating the violet LED die in silicone and curing to create an encapsulated device.
The process of Example 11, further comprising an additional cavity opening step being performed after the violet LED die have been coated with a first luminescent material and further coating the violet LED die with a second luminescent material.
The process of Example 11, further comprising forming through-hole vias in the submount.
The process of Example 25, further comprising dicing luminescent-material-coated die out of the submount as stand-alone LEDs.
The process of Example 11, wherein a reflective dam is placed around a set of luminescent-material-coated die.
The process of Example 11, wherein the layer of luminescent material is about 50 μm thick to about 450 μm thick.
The process of Example 11, further comprising dispensing silicone onto the layer of luminescent material.
The process of Example 11, further comprising mixing the luminescent materials with solvent followed by dispensing of silicone onto the luminescent materials.
The process of Example 11, further comprising mixing the luminescent materials with silicone prior to dispensing the layer of luminescent materials into the cavity holes.
A light source is formed using violet-emitting LED die arranged in a n×m array where n>m, then:
The light source of Example 32 where the violet-emitting LED die are grown on bulk GaN substrates.
The light source of Example 32 where the white-light-transparent dam material is loaded with a small number of scattering centers to improve the off-state appearance of the source and/or alter the light-emission pattern.
The light source of Example 32 where the violet-emitting LED die are individually coated with a conformal luminescent-material layer prior to placement of the white-light-transparent dams.
The light source of Example 35 where a white-light-transparent silicone is dispensed around the conformally-coated die and on top of the dam to create a lens cap.
A method of creating encapsulated, violet-die-based, white-emitting linear light sources by following the steps of:
The method of Example 37 where the violet-emitting LED die are grown on bulk GaN substrates.
The method of Example 37 where the white-light-transparent dam material is loaded with a small number of scattering centers to improve the off-state appearance of the source and/or alter the light-emission pattern.
The method of Example 37 where the violet-emitting LED die are individually coated with a conformal luminescent-material layer prior to placement of the white-light-transparent dams.
The method of Example 40 where a white-light-transparent silicone is dispensed around the conformally-coated violet LED die and on top of the dam to create a lens cap.
FIG. 16A1 through
The total light emitting surface (LES) of the LEDs and any down-conversion materials can form a light source 16A30. One or more light sources can be interconnected into an array 16B20, which in turn is in electrical contact with connectors 16B10 and brought into an assembly 16B30. One or more lens elements 16B40 can be optically coupled to the light source. The lens design and properties can be selected so that the desired directional beam pattern for a lighting product is achieved for a given LES. The directional lighting product may be an LED module, a retrofit lamp 16B70, or a lighting fixture 16C30. In the case of a retrofit lamp, an electronic driver can be provided with a surrounding member 16B60, the driver to condition electrical power from an external source to render it suitable for the LED light source. The driver can be integrated into the retrofit lamp. In the case of a fixture, an electronic driver is provided which conditions electrical power from an external source to make it suitable for the LED light source, with the driver either integrated into the fixture or provided externally to the fixture. In the case of a module, an electronic driver can be provided to condition electrical power from an external source to render it suitable for the LED light source, with the driver either integrated into the module or provided externally to the module. Examples of suitable external power sources include mains AC (e.g., 120 Vrms AC or 240 Vrms AC), low-voltage AC (e.g., 12 VAC), and low-voltage DC (e.g., 12 VDC). In the case of retrofit lamps, the entire lighting product may be designed to fit standard form factors (e.g., ANSI form factors). Examples of retrofit lamp products include LED-based MR16, PAR16, PAR20, PAR30, PAR38, BR30, A19 and various other lamp types. Examples of fixtures include replacements for halogen-based and ceramic metal halide-based directional lighting fixtures.
In some embodiments, the present disclosure can be applied to non-directional lighting applications. In these embodiments, one or more light-emitting diodes (LEDs), as taught by the disclosure, can be mounted on a submount or package to provide an electrical interconnection. The submount or package can be, for example, a ceramic, oxide, nitride, semiconductor, metal, or combination of any of the foregoing that includes electrical interconnection capability for the various LEDs. The submount or package can be mounted to a heatsink member via a thermal interface. The LEDs can be configured to produce a desired emission spectrum, either by mixing primary emissions from various LEDs, or by having the LEDs photo-excite wavelength down-conversion materials such as phosphors, semiconductors, or semiconductor nanoparticles (“quantum dots”), or a combination thereof. The LEDs can be distributed to provide a desired shape of the light source. For example, one common shape is a linear light source for replacement of conventional fluorescent linear tube lamps. One or more optical elements can be coupled to the LEDs to provide a desired non-directional light distribution. The non-directional lighting product may be an LED module, a retrofit lamp, or a lighting fixture. In the case of a retrofit lamp, an electronic driver can be provided to condition electrical power from an external source to render it suitable for the LED light source, with the driver integrated into the retrofit lamp. In the case of a fixture, an electronic driver is provided to condition electrical power from an external source to render it suitable for the LED light source, with the driver either integrated into the fixture or provided externally to the fixture. In the case of a module, an electronic driver can be provided to condition electrical power from an external source to render it suitable for the LED light source, with the driver either integrated into the module or provided externally to the module. Examples of external power sources include mains AC (e.g., 120 Vrms AC or 240 Vrms AC), low-voltage AC (e.g., 12 VAC), and low-voltage DC (e.g., 12 VDC). In the case of retrofit lamps, the entire lighting product may be designed to fit standard form factors (e.g., ANSI form factors). Examples of retrofit lamp products include LED-based replacements for various linear, circular, or curved fluorescent lamps. An example of a non-directional lighting product is shown in
Some embodiments of the present disclosure can be applied to backlighting for flat panel display applications. In these embodiments, one or more light-emitting diodes (LEDs), as taught by this disclosure, can be mounted on a submount or package to provide an electrical interconnection. The submount or package can be a ceramic, oxide, nitride, semiconductor, metal, or combination of any of the foregoing that include electrical interconnection capability for the various LEDs. The submount or package can be mounted to a heatsink member via a thermal interface. The LEDs can be configured to produce a desired emission spectrum, either by mixing primary emissions from various LEDs, or by having the LEDs photo-excite wavelength down-conversion materials such as phosphors, semiconductors, or semiconductor nanoparticles (“quantum dots”), or a combination of any of the foregoing. The LEDs can be distributed to provide a desired shape of the light source. One common shape is a linear light source. The light source can be optically coupled to a lightguide for the backlight. This can be achieved by coupling at the edge of the lightguide (edge-lit), or by coupling light from behind the lightguide (direct-lit). The lightguide distributes light uniformly toward a controllable display such as a liquid crystal display (LCD) panel. The display converts the LED light into desired images based on electrical control of light transmission and its color. One way to control the color is by use of filters (e.g., color filter substrate 16D40). Alternatively, multiple LEDs may be used and driven in pulsed mode to sequence the desired primary emission colors (e.g., using a red LED 16D30, a green LED 16D10, and a blue LED 16D20). Optional brightness-enhancing films may be included in the backlight “stack”. The brightness-enhancing films narrow the flat panel display emission to increase brightness at the expense of the observer viewing angle. An electronic driver can be provided to condition electrical power from an external source to render it suitable for the LED light source for backlighting, including any color sequencing or brightness variation per LED location (e.g., one-dimensional or two-dimensional dimming). Examples of external power sources include mains AC (e.g., 120 Vrms AC or 240 Vrms AC), low-voltage AC (e.g., 12 VAC), and low-voltage DC (e.g., 12 VDC). Examples of backlighting products are shown in FIG. 16D1, FIG. 16D2, FIG. 16E1 and FIG. 16E2.
Some embodiments of the present disclosure can be applied to automotive forward lighting applications, as shown in
In some embodiments, the present disclosure can be applied to digital imaging applications such as illumination for mobile phone and digital still cameras (e.g., see
Some embodiments of the present disclosure can be applied to mobile terminal applications.
In an example, the smart phone may include one or more of the following features (which are found in an iPhone 4 from Apple Inc., although there can be variations), see www.apple.com:
Embodiments of the present disclosure may be used with other electronic devices. Examples of suitable electronic devices include a portable electronic device such as a media player, a cellular phone, a personal data organizer, or the like. In such embodiments, a portable electronic device may include a combination of the functionalities of such devices. In addition, an electronic device may allow a user to connect to and communicate through the Internet or through other networks such as local or wide area networks. For example, a portable electronic device may allow a user to access the internet and to communicate using e-mail, text messaging, instant messaging, or using other forms of electronic communication. By way of example, the electronic device may be similar to an iPod having a display screen or an iPhone available from Apple Inc.
In certain embodiments, a device may be powered by one or more rechargeable and/or replaceable batteries. Such embodiments may be highly portable, allowing a user to carry the electronic device while traveling, working, exercising, and so forth. In this manner, and depending on the functionalities provided by the electronic device, a user may listen to music, play games or video, record video or take pictures, place and receive telephone calls, communicate with others, control other devices (e.g., via remote control and/or Bluetooth functionality), and so forth while moving freely with the device. In addition, the device may be sized such that it fits relatively easily into a pocket or the hand of the user. While certain embodiments of the present disclosure are described with respect to portable electronic devices, it should be noted that the presently disclosed techniques may be applicable to a wide array of other, less portable, electronic devices and systems that are configured to render graphical data such as a desktop computer.
As shown,
In some examples, instructions can be input to the handheld electronic device through an input device 16H24 that instructs the processor 16H08 to execute functions in an electronic imaging application. One potential instruction can be to generate an abstract of a captured image of a portion of a human user. In that case the processor 16H08 instructs the communications interface 16H11 to communicate with the server 16H02 (e.g., possibly through or using a cloud 16H04) and transfer data (e.g., image data). The data is transferred by the communications interface 16H11 and either processed by the processor 16H08 immediately after image capture or stored in memory 16H10 for later use, or both. The processor 16H08 also receives information regarding the display screen's attributes, and can calculate the orientation of the device, e.g., using information from an accelerometer 16H14 and/or other external data such as compass headings from a compass 16H18, or GPS location from a GPS chip 16H20, and the processor then uses the information to determine an orientation in which to display the image depending upon the example.
The captured image can be rendered by the processor 16H08, by a graphics accelerator 16H12, or by a combination of the two. In some embodiments, the processor can be the graphics accelerator 16H12. The image can first be stored in memory 16H10 or, if available, the memory can be directly associated with the graphics accelerator 16H12. The methods described herein can be implemented by the processor 16H08, the graphics accelerator 16H12, or a combination of the two to create the image and related abstract. An image or abstract can be displayed on the display screen 16H22.
The display may be a liquid crystal display (LCD), a light emitting diode (LED) based display, an organic light emitting diode (OLED) based display, or some other suitable display. In accordance with certain embodiments of the present disclosure, the display may display a user interface and various other images such as logos, avatars, photos, album art, and the like. Additionally, in certain embodiments, a display may include a touch screen through which a user may interact with the user interface. The display may also include various functions and/or system indicators to provide feedback to a user such as power status, call status, memory status, or the like. These indicators may be incorporated into the user interface displayed on the display.
In certain embodiments, one or more of the user input structures can be configured to control the device such as by controlling a mode of operation, an output level, an output type, etc. For instance, the user input structures may include a button to turn the device on or off. Further, the user input structures may allow a user to interact with the user interface on the display. Embodiments of the portable electronic device may include any number of user input structures including buttons, switches, a control pad, a scroll wheel, or any other suitable input structures. The user input structures may work with the user interface displayed on the device to control functions of the device and/or any interfaces or devices connected to or used by the device. For example, the user input structures may allow a user to navigate a displayed user interface or to return such a displayed user interface to a default or home screen.
Certain device may also include various input and output ports to allow connection of additional devices. For example, a port may be a headphone jack that provides for the connection of headphones. Additionally, a port may have both input and output capabilities to provide for the connection of a headset (e.g., a headphone and microphone combination). Embodiments of the present disclosure may include any number of input and/or output ports such as headphone and headset jacks, universal serial bus (USB) ports, IEEE-1394 ports, and AC and/or DC power connectors. Further, a device may use the input and output ports to connect to and send or receive data with any other device such as other portable electronic devices, personal computers, printers, or the like. For example, in one embodiment, the device may connect to a personal computer via an IEEE-1394 connection to send and receive data files such as media files.
The depiction of an electronic device 16I00 encompasses a smart phone system diagram according to an embodiment of the present disclosure. The depiction of an electronic device 16I00 illustrates computer hardware, software, and firmware that can be used to implement the disclosures above. The shown system includes a processor 16I26, which is representative of any number of physically and/or logically distinct resources capable of executing software, firmware, and hardware configured to perform identified computations. A processor 16I26 communicates with a chipset 16I28 that can control input to and output from processor 16I26. In this example, chipset 16I28 outputs information to display screen 16I42 and can read and write information to non-volatile storage 16I44, which can include magnetic media and solid state media, and/or other non-transitory media, for example. Chipset 16I28 can also read data from and write data to RAM 16I46. A bridge 16I32 for interfacing with a variety of user interface components can be provided for interfacing with chipset 16I28. Such user interface components can include a keyboard 16I34, a microphone 16I36, touch-detection-and-processing circuitry 16I38, a pointing device 16I40 such as a mouse, and so on. In general, inputs to the system can come from any of a variety of machine-generated and/or human-generated sources.
Chipset 16I28 also can interface with one or more data network interfaces 16I30 that can have different physical interfaces. Such data network interfaces 16I30 can include interfaces for wired and wireless local area networks, for broadband wireless networks, as well as personal area networks. Some applications of the methods for generating, displaying and using the GUI disclosed herein can include receiving data over a physical interface 16I31 or be generated by the machine itself by a processor 16I26 analyzing data stored in non-volatile storage 16I44 and/or in memory or RAM 16I46. Further, the machine can receive inputs from a user via devices such as a keyboard 16I34, microphone 16I36, touch-detection-and-processing circuitry 16I38, and pointing device 16I40 and execute appropriate functions such as browsing functions by interpreting these inputs using processor 16I26.
Additionally, the base member of a lamp can be of any form factor configured to support electrical connections, which electrical connections can conform to any of a set of types or standards. For example Table 3 gives standards (see “Type”) and corresponding characteristics, including mechanical spacing between a first pin (e.g., a power pin) and a second pin (e.g., a ground pin).
The listings above are merely representative and should not be taken to include all the standards or form factors that may be utilized within the scope of the embodiments described herein.
Finally, it should be noted that there are alternative ways of implementing the embodiments disclosed herein. Accordingly, the present embodiments are to be considered as illustrative and not restrictive, and the claims are not to be limited to the details given herein, but may be modified within the scope and equivalents thereof.
This application claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Application No. 61/740,937, filed on Dec. 21, 2012.
Number | Name | Date | Kind |
---|---|---|---|
3283143 | Gosnell | Nov 1966 | A |
3621233 | Ferdinand et al. | Nov 1971 | A |
4066868 | Witkin et al. | Jan 1978 | A |
4225904 | Linder | Sep 1980 | A |
4350560 | Helgeland et al. | Sep 1982 | A |
4581646 | Kubodera | Apr 1986 | A |
4873696 | Coldren et al. | Oct 1989 | A |
5005109 | Carleton | Apr 1991 | A |
5142387 | Shikama et al. | Aug 1992 | A |
5169486 | Young et al. | Dec 1992 | A |
5449930 | Zhou | Sep 1995 | A |
5523589 | Edmond et al. | Jun 1996 | A |
5536953 | Dreifus et al. | Jul 1996 | A |
5560700 | Levens | Oct 1996 | A |
5813753 | Vriens et al. | Sep 1998 | A |
6150774 | Mueller et al. | Nov 2000 | A |
6275145 | Rogozinski | Aug 2001 | B1 |
6300557 | Wanlass | Oct 2001 | B1 |
6335771 | Hiraishi | Jan 2002 | B1 |
6498355 | Harrah et al. | Dec 2002 | B1 |
6498440 | Stam et al. | Dec 2002 | B2 |
6509651 | Matsubara et al. | Jan 2003 | B1 |
6573537 | Steigerwald et al. | Jun 2003 | B1 |
6613461 | Sugahara | Sep 2003 | B1 |
6853010 | Slater, Jr. et al. | Feb 2005 | B2 |
6860628 | Robertson et al. | Mar 2005 | B2 |
6864641 | Dygert | Mar 2005 | B2 |
6889006 | Kobayashi | May 2005 | B2 |
6956246 | Epler et al. | Oct 2005 | B1 |
6967116 | Negley | Nov 2005 | B2 |
6989807 | Chiang | Jan 2006 | B2 |
7005679 | Tarsa et al. | Feb 2006 | B2 |
7009199 | Hall | Mar 2006 | B2 |
7027015 | Booth, Jr. et al. | Apr 2006 | B2 |
7038399 | Lys et al. | May 2006 | B2 |
7067985 | Adachi | Jun 2006 | B2 |
7067995 | Gunter et al. | Jun 2006 | B2 |
7081722 | Huynh et al. | Jul 2006 | B1 |
7083302 | Chen et al. | Aug 2006 | B2 |
7095056 | Vitta et al. | Aug 2006 | B2 |
7113658 | Ide et al. | Sep 2006 | B2 |
7148515 | Huang et al. | Dec 2006 | B1 |
7173384 | Plotz et al. | Feb 2007 | B2 |
7183577 | Mueller-Mach et al. | Feb 2007 | B2 |
7211822 | Nagahama et al. | May 2007 | B2 |
7213940 | Van De Ven et al. | May 2007 | B1 |
7233831 | Blackwell | Jun 2007 | B2 |
7250715 | Mueller et al. | Jul 2007 | B2 |
7252408 | Mazzochette et al. | Aug 2007 | B2 |
7253446 | Sakuma et al. | Aug 2007 | B2 |
7279040 | Wang | Oct 2007 | B1 |
7318651 | Chua et al. | Jan 2008 | B2 |
7352138 | Lys et al. | Apr 2008 | B2 |
7358543 | Chua et al. | Apr 2008 | B2 |
7358679 | Lys et al. | Apr 2008 | B2 |
7361938 | Mueller et al. | Apr 2008 | B2 |
7419281 | Porchia et al. | Sep 2008 | B2 |
7521862 | Mueller et al. | Apr 2009 | B2 |
7560981 | Chao et al. | Jul 2009 | B2 |
7564180 | Brandes | Jul 2009 | B2 |
7622742 | Kim et al. | Nov 2009 | B2 |
7646033 | Tran et al. | Jan 2010 | B2 |
7846757 | Farrell, Jr. et al. | Dec 2010 | B2 |
7858408 | Mueller et al. | Dec 2010 | B2 |
7884538 | Mitsuishi et al. | Feb 2011 | B2 |
7902564 | Mueller-Mach et al. | Mar 2011 | B2 |
7906793 | Negley | Mar 2011 | B2 |
7997774 | Liddle | Aug 2011 | B2 |
8044412 | Murphy et al. | Oct 2011 | B2 |
8044609 | Liu | Oct 2011 | B2 |
8062726 | Greiner et al. | Nov 2011 | B2 |
8124996 | Raring et al. | Feb 2012 | B2 |
8207554 | Shum | Jun 2012 | B2 |
8269245 | Shum | Sep 2012 | B1 |
8299473 | D'Evelyn et al. | Oct 2012 | B1 |
8310143 | Van De Ven et al. | Nov 2012 | B2 |
8324840 | Shteynberg et al. | Dec 2012 | B2 |
8362603 | Lim et al. | Jan 2013 | B2 |
8399898 | Jagt et al. | Mar 2013 | B2 |
8404071 | Cope et al. | Mar 2013 | B2 |
8410711 | Lin et al. | Apr 2013 | B2 |
8410717 | Shteynberg et al. | Apr 2013 | B2 |
8431942 | Butterworth | Apr 2013 | B2 |
8476644 | Illek et al. | Jul 2013 | B2 |
8502465 | Katona et al. | Aug 2013 | B2 |
8519437 | Chakraborty | Aug 2013 | B2 |
8525396 | Shum et al. | Sep 2013 | B2 |
8541951 | Shum et al. | Sep 2013 | B1 |
8575642 | Shum | Nov 2013 | B1 |
D694722 | Shum et al. | Dec 2013 | S |
8618560 | D'Evelyn et al. | Dec 2013 | B2 |
8651711 | Rudisill et al. | Feb 2014 | B2 |
8674395 | Shum | Mar 2014 | B2 |
8686458 | Krames et al. | Apr 2014 | B2 |
8704258 | Tasaki et al. | Apr 2014 | B2 |
8740413 | Krames et al. | Jun 2014 | B1 |
8746918 | Rubino | Jun 2014 | B1 |
8752975 | Rubino | Jun 2014 | B2 |
8786053 | D'Evelyn et al. | Jul 2014 | B2 |
8791499 | Sharma et al. | Jul 2014 | B1 |
8829774 | Shum et al. | Sep 2014 | B1 |
8888332 | Martis et al. | Nov 2014 | B2 |
8896235 | Shum et al. | Nov 2014 | B1 |
8905588 | Krames et al. | Dec 2014 | B2 |
8933644 | David et al. | Jan 2015 | B2 |
9236414 | Matsuura | Jan 2016 | B2 |
20010022495 | Salam | Sep 2001 | A1 |
20010055208 | Kimura | Dec 2001 | A1 |
20020063258 | Motoki | May 2002 | A1 |
20020088985 | Komoto et al. | Jul 2002 | A1 |
20020190260 | Shen et al. | Dec 2002 | A1 |
20030012246 | Klimek et al. | Jan 2003 | A1 |
20030030063 | Sosniak et al. | Feb 2003 | A1 |
20040031437 | Sarayama et al. | Feb 2004 | A1 |
20040070004 | Eliashevich et al. | Apr 2004 | A1 |
20040080938 | Holman et al. | Apr 2004 | A1 |
20040100192 | Yano | May 2004 | A1 |
20040104391 | Maeda et al. | Jun 2004 | A1 |
20040135136 | Takahashi et al. | Jul 2004 | A1 |
20040164308 | Asatsuma et al. | Aug 2004 | A1 |
20040190304 | Sugimoto et al. | Sep 2004 | A1 |
20040201598 | Eliav et al. | Oct 2004 | A1 |
20040207998 | Suehiro et al. | Oct 2004 | A1 |
20040227149 | Ibbetson et al. | Nov 2004 | A1 |
20040251471 | Dwilinski et al. | Dec 2004 | A1 |
20050024744 | Falicoff et al. | Feb 2005 | A1 |
20050030760 | Capello et al. | Feb 2005 | A1 |
20050057145 | Shieh | Mar 2005 | A1 |
20050084218 | Ide et al. | Apr 2005 | A1 |
20050087753 | D'Evelyn et al. | Apr 2005 | A1 |
20050109240 | Maeta et al. | May 2005 | A1 |
20050140270 | Henson et al. | Jun 2005 | A1 |
20050179376 | Fung et al. | Aug 2005 | A1 |
20050199899 | Lin et al. | Sep 2005 | A1 |
20050224830 | Blonder et al. | Oct 2005 | A1 |
20050225988 | Chaves et al. | Oct 2005 | A1 |
20050232327 | Nomura et al. | Oct 2005 | A1 |
20050253158 | Yasukawa | Nov 2005 | A1 |
20060006404 | Ibbetson et al. | Jan 2006 | A1 |
20060038542 | Park et al. | Feb 2006 | A1 |
20060060872 | Edmond et al. | Mar 2006 | A1 |
20060065900 | Hsieh et al. | Mar 2006 | A1 |
20060068154 | Parce et al. | Mar 2006 | A1 |
20060078022 | Kozaki et al. | Apr 2006 | A1 |
20060097385 | Negley | May 2006 | A1 |
20060105485 | Basin et al. | May 2006 | A1 |
20060108162 | Tabata et al. | May 2006 | A1 |
20060118799 | D'Evelyn et al. | Jun 2006 | A1 |
20060124051 | Yoshioka et al. | Jun 2006 | A1 |
20060149607 | Sayers et al. | Jul 2006 | A1 |
20060152795 | Yang | Jul 2006 | A1 |
20060177362 | D'Evelyn et al. | Aug 2006 | A1 |
20060180828 | Kim et al. | Aug 2006 | A1 |
20060208262 | Sakuma et al. | Sep 2006 | A1 |
20060226759 | Masuda et al. | Oct 2006 | A1 |
20060261364 | Suehiro et al. | Nov 2006 | A1 |
20060262545 | Piepgras et al. | Nov 2006 | A1 |
20060273339 | Steigerwald et al. | Dec 2006 | A1 |
20060288927 | Chodelka et al. | Dec 2006 | A1 |
20070007898 | Bruning | Jan 2007 | A1 |
20070012944 | Bader et al. | Jan 2007 | A1 |
20070072324 | Krames et al. | Mar 2007 | A1 |
20070091608 | Hauffe et al. | Apr 2007 | A1 |
20070104861 | Chen | May 2007 | A1 |
20070114561 | Comanzo et al. | May 2007 | A1 |
20070114563 | Paek et al. | May 2007 | A1 |
20070126023 | Haskell et al. | Jun 2007 | A1 |
20070139920 | Van De Ven et al. | Jun 2007 | A1 |
20070170450 | Murphy | Jul 2007 | A1 |
20070181895 | Nagai | Aug 2007 | A1 |
20070202624 | Yoon et al. | Aug 2007 | A1 |
20070210074 | Maurer et al. | Sep 2007 | A1 |
20070228404 | Tran et al. | Oct 2007 | A1 |
20070231963 | Doan et al. | Oct 2007 | A1 |
20070240346 | Li et al. | Oct 2007 | A1 |
20070257272 | Hutchins | Nov 2007 | A1 |
20080006837 | Park et al. | Jan 2008 | A1 |
20080048200 | Mueller et al. | Feb 2008 | A1 |
20080054290 | Shieh et al. | Mar 2008 | A1 |
20080083741 | Giddings et al. | Apr 2008 | A1 |
20080087919 | Tysoe et al. | Apr 2008 | A1 |
20080099777 | Erchak et al. | May 2008 | A1 |
20080108162 | Dwilinski et al. | May 2008 | A1 |
20080116786 | Wang et al. | May 2008 | A1 |
20080151543 | Wang | Jun 2008 | A1 |
20080158887 | Zhu et al. | Jul 2008 | A1 |
20080173882 | Parikh et al. | Jul 2008 | A1 |
20080173884 | Chitnis et al. | Jul 2008 | A1 |
20080179607 | DenBaars et al. | Jul 2008 | A1 |
20080179611 | Chitnis et al. | Jul 2008 | A1 |
20080187746 | De Graaf et al. | Aug 2008 | A1 |
20080192791 | Furukawa et al. | Aug 2008 | A1 |
20080194054 | Lin et al. | Aug 2008 | A1 |
20080203419 | Harada | Aug 2008 | A1 |
20080206925 | Chatterjee et al. | Aug 2008 | A1 |
20080211389 | Oshio | Sep 2008 | A1 |
20080218759 | Colvin et al. | Sep 2008 | A1 |
20080258165 | Zimmerman et al. | Oct 2008 | A1 |
20080272463 | Butcher et al. | Nov 2008 | A1 |
20080284346 | Lee | Nov 2008 | A1 |
20090008573 | Conner | Jan 2009 | A1 |
20090008648 | Biwa | Jan 2009 | A1 |
20090032828 | Romano et al. | Feb 2009 | A1 |
20090045439 | Hoshi et al. | Feb 2009 | A1 |
20090050908 | Yuan et al. | Feb 2009 | A1 |
20090071394 | Nakahata et al. | Mar 2009 | A1 |
20090081857 | Hanser et al. | Mar 2009 | A1 |
20090140279 | Zimmerman et al. | Jun 2009 | A1 |
20090146170 | Zhong et al. | Jun 2009 | A1 |
20090162963 | Tansu et al. | Jun 2009 | A1 |
20090173958 | Chakraborty et al. | Jul 2009 | A1 |
20090184624 | Schmidt et al. | Jul 2009 | A1 |
20090191658 | Kim et al. | Jul 2009 | A1 |
20090194796 | Hashimoto et al. | Aug 2009 | A1 |
20090206354 | Kitano et al. | Aug 2009 | A1 |
20090212277 | Akita et al. | Aug 2009 | A1 |
20090213120 | Nisper et al. | Aug 2009 | A1 |
20090221106 | Zimmerman et al. | Sep 2009 | A1 |
20090226139 | Yuang | Sep 2009 | A1 |
20090227056 | Kyono et al. | Sep 2009 | A1 |
20090262516 | Li | Oct 2009 | A1 |
20090272996 | Chakraborty | Nov 2009 | A1 |
20090273005 | Lin | Nov 2009 | A1 |
20090309105 | Letts et al. | Dec 2009 | A1 |
20090315057 | Konishi | Dec 2009 | A1 |
20090315480 | Yan et al. | Dec 2009 | A1 |
20090321778 | Chen et al. | Dec 2009 | A1 |
20100001300 | Raring et al. | Jan 2010 | A1 |
20100025656 | Raring et al. | Feb 2010 | A1 |
20100031875 | D'Evelyn | Feb 2010 | A1 |
20100041170 | Epler et al. | Feb 2010 | A1 |
20100051974 | Krames | Mar 2010 | A1 |
20100055819 | Ohba et al. | Mar 2010 | A1 |
20100059767 | Kawasaki | Mar 2010 | A1 |
20100060130 | Li | Mar 2010 | A1 |
20100067241 | Lapatovich et al. | Mar 2010 | A1 |
20100109025 | Bhat | May 2010 | A1 |
20100117106 | Trottier | May 2010 | A1 |
20100140634 | van de Ven et al. | Jun 2010 | A1 |
20100148210 | Huang et al. | Jun 2010 | A1 |
20100149814 | Zhai et al. | Jun 2010 | A1 |
20100155746 | Ibbetson et al. | Jun 2010 | A1 |
20100164403 | Liu | Jul 2010 | A1 |
20100200888 | Kuhmann et al. | Aug 2010 | A1 |
20100226399 | Nishinaka | Sep 2010 | A1 |
20100226404 | Kim et al. | Sep 2010 | A1 |
20100240158 | Ter-Hovhannissian | Sep 2010 | A1 |
20100244055 | Greisen | Sep 2010 | A1 |
20100258830 | Ide et al. | Oct 2010 | A1 |
20100290208 | Pickard | Nov 2010 | A1 |
20100291313 | Ling | Nov 2010 | A1 |
20100315012 | Kim | Dec 2010 | A1 |
20110001157 | McKenzie et al. | Jan 2011 | A1 |
20110018026 | Konno | Jan 2011 | A1 |
20110025183 | Su | Feb 2011 | A1 |
20110038154 | Chakravarty et al. | Feb 2011 | A1 |
20110057205 | Mueller et al. | Mar 2011 | A1 |
20110062415 | Ohta et al. | Mar 2011 | A1 |
20110064103 | Ohta et al. | Mar 2011 | A1 |
20110068700 | Fan | Mar 2011 | A1 |
20110101350 | Greisen | May 2011 | A1 |
20110121331 | Simonian et al. | May 2011 | A1 |
20110136281 | Sheen | Jun 2011 | A1 |
20110140150 | Shum | Jun 2011 | A1 |
20110181173 | De Graaf et al. | Jul 2011 | A1 |
20110182056 | Trottier et al. | Jul 2011 | A1 |
20110182065 | Negley et al. | Jul 2011 | A1 |
20110186874 | Shum | Aug 2011 | A1 |
20110198566 | Yoshizumi | Aug 2011 | A1 |
20110198979 | Shum et al. | Aug 2011 | A1 |
20110204763 | Shum et al. | Aug 2011 | A1 |
20110204779 | Shum et al. | Aug 2011 | A1 |
20110204780 | Shum et al. | Aug 2011 | A1 |
20110215348 | Trottier et al. | Sep 2011 | A1 |
20110223701 | Kyono et al. | Sep 2011 | A1 |
20110260188 | Choi et al. | Oct 2011 | A1 |
20110266552 | Tu et al. | Nov 2011 | A1 |
20110279998 | Su et al. | Nov 2011 | A1 |
20110317397 | Trottier et al. | Dec 2011 | A1 |
20120012856 | Chen et al. | Jan 2012 | A1 |
20120043552 | David et al. | Feb 2012 | A1 |
20120044667 | Hanawa | Feb 2012 | A1 |
20120061702 | Andrews | Mar 2012 | A1 |
20120061709 | Pachler | Mar 2012 | A1 |
20120086022 | Veerasamy et al. | Apr 2012 | A1 |
20120086023 | Veerasamy et al. | Apr 2012 | A1 |
20120086024 | Andrews | Apr 2012 | A1 |
20120088319 | Veerasamy et al. | Apr 2012 | A1 |
20120091465 | Krames et al. | Apr 2012 | A1 |
20120092853 | Daicho | Apr 2012 | A1 |
20120161163 | Kim | Jun 2012 | A1 |
20120187830 | Shum et al. | Jul 2012 | A1 |
20120187862 | Britt | Jul 2012 | A1 |
20120235201 | Shum | Sep 2012 | A1 |
20120250310 | Hussell | Oct 2012 | A1 |
20120292649 | Sugiyama et al. | Nov 2012 | A1 |
20120299051 | Jeong | Nov 2012 | A1 |
20120299492 | Egawa et al. | Nov 2012 | A1 |
20120313541 | Egawa et al. | Dec 2012 | A1 |
20120319148 | Donofrio | Dec 2012 | A1 |
20120320309 | Hineno | Dec 2012 | A1 |
20130020590 | Lin | Jan 2013 | A1 |
20130020601 | Daicho | Jan 2013 | A1 |
20130022758 | Trottier | Jan 2013 | A1 |
20130026483 | Sharma et al. | Jan 2013 | A1 |
20130043799 | Siu et al. | Feb 2013 | A1 |
20130050979 | Van De Ven | Feb 2013 | A1 |
20130075773 | Kijima | Mar 2013 | A1 |
20130119417 | Andrews | May 2013 | A1 |
20130119426 | Katoh | May 2013 | A1 |
20130126927 | Iguchi | May 2013 | A1 |
20130207148 | Krauter et al. | Aug 2013 | A1 |
20130234108 | David et al. | Sep 2013 | A1 |
20130292728 | Ishimori et al. | Nov 2013 | A1 |
20130313516 | David et al. | Nov 2013 | A1 |
20130322089 | Martis et al. | Dec 2013 | A1 |
20130323490 | D'Evelyn et al. | Dec 2013 | A1 |
20140027789 | Katona et al. | Jan 2014 | A1 |
20140042918 | Lee | Feb 2014 | A1 |
20140070710 | Harris | Mar 2014 | A1 |
20140091697 | Shum | Apr 2014 | A1 |
20140103356 | Krames et al. | Apr 2014 | A1 |
20140119007 | Edmond | May 2014 | A1 |
20140145235 | Shum | May 2014 | A1 |
20140175377 | D'Evelyn | Jun 2014 | A1 |
20140218909 | Tetsuo | Aug 2014 | A1 |
20140225137 | Krames et al. | Aug 2014 | A1 |
20140301062 | David et al. | Oct 2014 | A1 |
20150049460 | David et al. | Feb 2015 | A1 |
20150062892 | Krames et al. | Mar 2015 | A1 |
20150155439 | Cich | Jun 2015 | A1 |
Number | Date | Country |
---|---|---|
2381490 | Oct 2011 | EP |
H02-028541 | Jan 1990 | JP |
H03-142963 | Jun 1991 | JP |
06-334215 | Dec 1994 | JP |
H09-199756 | Jul 1997 | JP |
2002-161000 | Jun 2002 | JP |
2004-179644 | Jun 2004 | JP |
2004-533391 | Nov 2004 | JP |
2005-217421 | Aug 2005 | JP |
2007-507115 | Mar 2006 | JP |
2006-147933 | Jun 2006 | JP |
2007-067418 | Mar 2007 | JP |
2007-103371 | Apr 2007 | JP |
2007-110090 | Apr 2007 | JP |
2007-331973 | Dec 2007 | JP |
2008-501600 | Jan 2008 | JP |
2008-084973 | Apr 2008 | JP |
2008-521737 | Jun 2008 | JP |
2008-172040 | Jul 2008 | JP |
2008-258503 | Oct 2008 | JP |
2008-263154 | Oct 2008 | JP |
2009-130097 | Jun 2009 | JP |
2010-517274 | Sep 2009 | JP |
2009-267164 | Nov 2009 | JP |
2010-034487 | Feb 2010 | JP |
2010-098068 | Apr 2010 | JP |
2010-212493 | Sep 2010 | JP |
2010-226110 | Oct 2010 | JP |
2010-263128 | Nov 2010 | JP |
2011-501351 | Jan 2011 | JP |
2011-051863 | Mar 2011 | JP |
2011-057763 | Mar 2011 | JP |
2011-068503 | Apr 2011 | JP |
2011-077325 | Apr 2011 | JP |
2011142254 | Jul 2011 | JP |
2011-148655 | Aug 2011 | JP |
2011-151419 | Aug 2011 | JP |
2010232525 | Oct 2011 | JP |
2011-219304 | Nov 2011 | JP |
2011-222760 | Nov 2011 | JP |
2011-230998 | Nov 2011 | JP |
2011-243963 | Dec 2011 | JP |
2012-001432 | Jan 2012 | JP |
2012-056970 | Mar 2012 | JP |
2012-064860 | Mar 2012 | JP |
2012-512119 | May 2012 | JP |
WO 2006062880 | Jun 2006 | WO |
WO 2008091846 | Jul 2008 | WO |
WO 2009001039 | Dec 2008 | WO |
WO 2009066430 | May 2009 | WO |
WO 2010119375 | Oct 2010 | WO |
WO 2010150880 | Dec 2010 | WO |
WO 2011010774 | Jan 2011 | WO |
WO 2011034226 | Mar 2011 | WO |
WO 2011035265 | Mar 2011 | WO |
WO 2011097393 | Aug 2011 | WO |
WO 2012022813 | Feb 2012 | WO |
WO 2012024636 | Feb 2012 | WO |
Entry |
---|
Mastro et al., ‘Hydride vapor phase epitaxy-grown AlGaN/GaN high electron mobility transistors’, Solid-State Electronics, vol. 47, Issue 6, Jun. 2003, pp. 1075-1079. |
Morkoc, ‘Handbook of Nitride Semiconductors and Devices’, vol. 1, 2008, p. 704. |
UPSTO Office Action for U.S. Appl. No. 13/135,087 dated Aug. 15, 2014 (12 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/973,213 dated Sep. 16, 2014 (7 pages). |
USPTO Office Action for U.S. Appl. No. 14/022,587 dated Jul. 30, 2014 (9 pages). |
USPTO Office Action for U.S. Appl. No. 14/054,234 dated Aug. 14, 2014 (24 pages). |
International Search Report of PCT Application No. PCT/US2011/023622, dated Apr. 1, 2011, 2 pages total. |
Saito et al., ‘Plane Dependent Growth of GaN in Supercritical Basic Ammonia’, Applied Physics Express, vol. 1, No. 12, Dec. 2008, pp. 121103-1-121103-3. |
Communication from the Japanese Patent Office re 2013-117510 dated Sep. 24, 2014 (8 pages). |
Zhong et al., ‘High Power and High Efficiency Blue Light Emitting Diode on Freestanding Semipolar (1011) Bulk GaN Substrate’, Applied Physics Letter, vol. 90, No. 23, 2007, pp. 233504-1-233504-3. |
Zhong et al., ‘Demonstration of High Power Blue-Green Light Emitting Diode on Semipolar (1122) Bulk GaN Substrate’, Electronics Letters, vol. 43, No. 15, 2007, pp. 825-826. |
USPTO Office Action for U.S. Appl. No. 13/019,897 dated Dec. 5, 2014 (18 pages). |
USPTO Office Action for U.S. Appl. No. 13/210,769 dated Oct. 10, 2014 (10 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/781,633 dated Nov. 28, 2014 (9 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/909,752 dated Sep. 30, 2014 (9 pages). |
Communication from the Japanese Patent Office re 2013-263760 dated Nov. 14, 2014 (11 pages). |
Caliper, ‘CALiPER Application Summary Report 22: LED MR16 Lamps’, Solid-State Lighting Program, Jun. 2014, pp. 1-25. |
Chhajed et al., ‘Junction temperature in light-emitting diodes assessed by different methods’, Future Chips Constellation, not dated, pp. 1-9. |
Cich et al., ‘Bulk GaN based violet light-emitting diodes with high efficiency at very high current density’, Applied Physics Letters, Nov. 29, 2012, pp. 223509-1-223509-3. |
Csuti et al., ‘Color-matching experiments with RGB-LEDs’, Color Research and Application, vol. 33, No. 2, 2008, pp. 1-9. |
David et al., ‘Carrier distribution in (0001)InGaN/GaN multiple quantam well light-emitting diodes’, Applied Physics Letters, vol. 92, No. 053502, Feb. 4, 2008, pp. 1-3. |
David et al., ‘Influence of polarization fields on carrier lifetime and recombination rates in InGaN-based light-emitting diodes’, Applied Physics Letters, vol. 97, No. 033501, Jul. 19, 2010, pp. 1-3. |
Davis et al., ‘Color quality scale’, Optical Engineering, vol. 49, No. 3, Mar. 2010, pp. 033602-1-036602-16. |
Gardner et al., ‘Blue-Emitting InGaN—GaN Double-Heterostructure Light-Emitting Diodes Reaching Maximum Quantum Efficiency Above 200 A/cm2’, Applied Physics Letters. vol. 91, 2007, pp. 243506-1-243506-3. |
Hayakawa et al., ‘Analysis of trace Co in synthetic diamonds using synchroton radiation excited X-ray fluorescence analysis’, Journal of Crystal Growth, vol. 210, Mar. 1, 2000, pp. 388-394. |
Houser et al., ‘Review of measures for light-source color rendition and considerations for a two-measure system for characterizing color rendition’, Optics Express, vol. 21, No. 8, Apr. 19, 2013, pp. 10393-10411. |
Paper and Board Determination of CIE Whiteness, D65/10 (outdoor daylight), ISO International Standard 11475:2004E (2004), 18 pgs. |
Kumar et al., ‘Guest Editorial Special Issue on Light-Emitting Diodes’, IEEE Transactions on Electron Devices, vol. 57, No. 1, Jan. 2010, pp. 7-11. |
Laufer et al., ‘Determination of secondary ion mass spectrometry relative sensitivity factors for polar and non-polar ZnO’, Journal of Applied Physics, vol. 110, 2011, pp. 094906-1-094906-5. |
Madelung, ‘III-V Compounds’, Semiconductors: Data Handbook, Springer Verlag, Berlin-Heidelberg, vol. 3, Ch. 2, 2004, pp. 71-172. |
Masui et al., ‘Electrical Characteristics of Nonpolar InGaN-Based Light-Emitting Diodes Evaluated at Low Temperature’, Japanese Journal of Applied Physics, vol. 46, No. 11, 2007, pp. 7309-7310. |
Michiue et al., ‘Recent Development of Nitride LEDs and LDs’, Proceedings of SPIE, vol. 7216, 2009, pp. 72161Z-1-72161Z-6. |
Narendran et al., ‘Color Rendering Properties of LED Light Sources’, Solid State Lighting II: Proceedings of SPIE, 2002, pp. 1-8. |
Narukawa et al., ‘White light emitting diodes with super-high luminous efficacy’, Journal of Physics D: Applied Physics, vol. 43, No. 354002, Aug. 19, 2010, pp. 1-6. |
http://www.philipslumileds.com/products/luxeon-flash, ‘LUXEON Flash’, Philips Lumileds, Aug. 8, 2013, pp. 1-2. |
Sato et al., ‘High Power and High Efficiency Semipolar InGaN Light Emitting Diodes’, Journal of Light and Visible Environment, vol. 32, No. 2, Dec. 13, 2007, pp. 57-60. |
Sato et al., ‘High Power and High Efficiency Semipolar InGaN Light Emitting Diodes’, Journal of Light and Visible Environment, vol. 32, No. 2, Feb. 12, 2008, pp. 107-110. |
Sekiguchi et al., ‘Hydrothermal growth of ZnO single crystals and their optical characterization’, Journal of Crystal Growth, vol. 214-215, Jun. 2, 2000, pp. 72-76. |
Shen et al., ‘Auger Recombination in Letters InGaN Measured by Photoluminescence’, Applied Physics Letters, vol. 91, 2007, pp. 141101-1-141101-3. |
Tomiya et al., ‘Dislocation Related Issues in the Degradation of GaN-Based Laser Diodes’, IEEE Journal of Selected Topics in Quantum Electronics, vol. 10, No. 6, 2004, pp. 1277-1287. |
Communication from the Chinese Patent Office re 201080052148.X dated Apr. 11, 2014 (5 pages). |
Communication from the Japanese Patent Office re 2012-529969 dated Jul. 4, 2014 (8 pages). |
Communication from the Japanese Patent Office re 2012-529969 dated Dec. 5, 2014 (2 pages). |
Communication from the Japanese Patent Office re 2012-5520086 dated Nov. 28, 2014 (6 pages). |
Communication from the Japanese Patent Office re 2013097298 dated Jun. 6, 2014 (7 pages). |
Communication from the Japanese Patent Office re 2012-529969, dated Oct. 15, 2013, (6 pages). |
Weaver et al., ‘Optical Properties of Selected Elements’, Handbook of Chemistry and Physics, vol. 94, 2013-2014, pp. 12-126-12-140. |
Whitehead et al., ‘A Monte Carlo method for assessing color rendering quality with possible application to color rendering standards’, Color Research and Application, vol. 37, No. 1, Feb. 2012, pp. 13-22. |
USPTO Office Action for U.S. Appl. No. 12/749,466 dated Jul. 3, 2012 (18 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/754,886 dated May 17, 2012 (19 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/754,886 dated Jun. 5, 2012 (16 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/754,886 dated Jun. 20, 2012 (14 pages). |
USPTO Office Action for U.S. Appl. No. 12/936,238 dated Aug. 30, 2012 (11 pages). |
USPTO Office Action for U.S. Appl. No. 12/936,238 dated Jan. 30, 2013 (12 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/936,238 dated Apr. 16, 2013 (9 pages). |
USPTO Office Action for U.S. Appl. No. 13/025,791 dated Nov. 25, 2011 (11 pages). |
USPTO Office Action for U.S. Appl. No. 13/025,791 dated Feb. 20, 2013 (13 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/025,791 dated Jun. 17, 2013 (8 pages). |
USPTO Office Action for U.S. Appl. No. 13/328,978 dated May 15, 2013 (24 pages). |
USPTO Office Action for U.S. Appl. No. 13/328,978 dated Sep. 26, 2013 (25 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/328,978 dated Mar. 18, 2014 (13 pages). |
USPTO Office Action for U.S. Appl. No. 13/357,315 dated Dec. 31, 2014 (22 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/623,788 dated Aug. 20, 2013 (11 pages). |
USPTO Office Action for U.S. Appl. No. 13/787,582 dated Jan. 22, 2015 (16 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/856,613 dated Nov. 21, 2014 (8 pages). |
USPTO Office Action for U.S. Appl. No. 13/904,237 dated Dec. 29, 2014 (20 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/931,359 dated Dec. 23, 2013 (10 pages). |
USPTO Office Action for U.S. Appl. No. 13/959,422 dated Oct. 8, 2013 (10 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/959,422 dated Jul. 9, 2014 (7 pages). |
USPTO Office Action for U.S. Appl. No. 14/054,234 dated Mar. 6, 2015 (20 pages). |
USPTO Office Action for U.S. Appl. No. 14/097,043 dated Oct. 15, 2014 (11 pages). |
USPTO Office Action for U.S. Appl. No. 14/191,950 dated Aug. 18, 2014 (7 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 14/256,670 dated Aug. 4, 2014 (12 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 14/256,670 dated Sep. 19, 2014 (2 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 14/310,957 dated Oct. 8, 2014 (9 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 14/310,957 dated Nov. 28, 2014 (6 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 14/528,876 dated Jan. 28, 2015 (8 pages). |
Benke et al., ‘Uncertainty in Health Risks from Artificial Lighting due to Disruption of Circadian Rythm and Melatonin Secretion: A Review’, Human and Ecological Risk Assessment: An International Journal, vol. 19, No. 4, 2013, p. 916-929. |
Hanifin et al., ‘Photoreception for Circadian, Neuroendocrine, and Neurobehavioral Regulation’, Journal of Physiological Anthropology, vol. 26, 2007, p. 87-94. |
Iso et al., ‘High Brightness Blue InGaN/GaN Light Emitting Diode on Nonpolar m-Plane Bulk GaN Substrate’, Japanese Journal of Applied Physics, vol. 46, No. 40, 2007, p. L960-L962. |
International Search Report & Written Opinion of PCT Application No. PCT/US2013/029453, dated Jul. 25, 2013, 11 pages total. |
Rea et al., ‘White Lighting’, Color Research and Application, vol. 38, No. 2, Sep. 3, 2011, p. 82-92. |
Sato et al., ‘Optical Properties of Yellow Light-Emitting Diodes Grown on Semipolar (1122) Bulk GaN Substrate’, Applied Physics Letters, vol. 92, No. 22, 2008, p. 221110-1-221110-3. |
Communication from the Chinese Patent Office re 200980134876.2 dated Mar. 6, 2014, (10 pages). |
Communication from the Japanese Patent Office re 2011-522191 dated Mar. 28, 2014, (6 pages). |
Communication from the Korean Patent Office re 10-2012-7009980 dated Apr. 15, 2013, (6 pages). |
Weaver et al., ‘Optical Properties of Selected Elements’, Handbook of Chemistry and Physics, 94th Edition, 2013-2014, p. 12-126-12-150. |
USPTO Office Action for U.S. Appl. No. 12/491,176 dated Mar. 1, 2012 (9 pages). |
USPTO Office Action for U.S. Appl. No. 12/491,176 dated Jul. 19, 2012 (13 pages). |
USPTO Office Action for U.S. Appl. No. 12/491,176 dated Nov. 22, 2013 (14 pages). |
USPTO Office Action for U.S. Appl. No. 12/879,784 dated Jan. 25, 2012 (6 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/879,784 dated Apr. 3, 2012 (7 pages). |
USPTO Office Action for U.S. Appl. No. 12/914,789 dated Oct. 12, 2011 (7 pages). |
USPTO Office Action for U.S. Appl. No. 12/914,789 dated Feb. 24, 2012 (8 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/914,789 dated May 17, 2012 (5 pages). |
USPTO Office Action for U.S. Appl. No. 13/019,897 dated Mar. 30, 2012 (14 pages). |
USPTO Office Action for U.S. Appl. No. 13/019,897 dated Jan. 16, 2013 (7 pages). |
USPTO Office Action for U.S. Appl. No. 13/019,897 dated Dec. 2, 2013 (17 pages). |
USPTO Office Action for U.S. Appl. No. 13/019,897 dated Jun. 12, 2014 (8 pages). |
USPTO Office Action for U.S. Appl. No. 13/025,833 dated Jul. 12, 2012 (15 pages). |
USPTO Office Action for U.S. Appl. No. 13/135,087 dated Sep. 27, 2013 (7 pages). |
USPTO Office Action for U.S. Appl. No. 13/210,769 dated Apr. 3, 2013 (13 pages). |
USPTO Office Action for U.S. Appl. No. 13/210,769 dated Oct. 28, 2013 (9 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/298,905 dated Jun. 11, 2013 (8 pages). |
USPTO Office Action for U.S. Appl. No. 13/357,315 dated Oct. 15, 2013 (12 pages). |
USPTO Office Action for U.S. Appl. No. 13/472,356 dated Dec. 9, 2013 (11 pages). |
USPTO Office Action for U.S. Appl. No. 13/472,356 dated Jun. 5, 2014 (12 pages). |
USPTO Office Action for U.S. Appl. No. 13/482,956 dated Aug. 17, 2012 (9 pages). |
USPTO Office Action for U.S. Appl. No. 13/482,956 dated Feb. 14, 2013 (15 pages). |
USPTO Office Action for U.S. Appl. No. 13/482,956 dated Jul. 22, 2013 (16 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/482,956 dated Oct. 28, 2013 (9 pages). |
USPTO Office Action for U.S. Appl. No. 13/600,988 dated Jul. 18, 2013 (12 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/600,988 dated Sep. 16, 2013 (9 pages). |
USPTO Office Action for U.S. Appl. No. 13/781,633 dated Mar. 6, 2014 (11 pages). |
USPTO Office Action for U.S. Appl. No. 13/904,237 dated May 22, 2014 (13 pages). |
USPTO Office Action for U.S. Appl. No. 14/171,885 dated Mar. 28, 2014 (8 pages). |
Number | Date | Country | |
---|---|---|---|
20140175492 A1 | Jun 2014 | US |
Number | Date | Country | |
---|---|---|---|
61740937 | Dec 2012 | US |