Method for manufacture of bright GaN LEDs using a selective removal process

Information

  • Patent Grant
  • 8912025
  • Patent Number
    8,912,025
  • Date Filed
    Wednesday, November 23, 2011
    13 years ago
  • Date Issued
    Tuesday, December 16, 2014
    10 years ago
Abstract
A method of fabricating LED devices includes using a laser to form trenches between the LEDs and then using a chemical solution to remove slag creating by the laser.
Description
BACKGROUND OF THE INVENTION

The present invention generally relates to semiconductor processes and, more particularly, to a method for singulating die from a wafer in furtherance of fabricating light emitting diodes.


Although saw dicing has traditionally been effectively used for singulating dice it has given way to singulation processes employing different methods. For example the laser has replaced the mechanical saw to avoid the deleterious effects of vibration and particulate contaminates generated by saw dicing. Edge defects that often occurred as a result of saw dicing are avoided, as are micro-cracks.


Laser cutting may be employed with a cleaving process such that the laser is used to form a trench in the wafer, but does not cut completely through the wafer. A cleaving process is implemented to complete the singulation process after formation of the trench. Often the laser cutting process leaves a residue on the die formed from the singulation process. The residue may prove problematic to the desired operation of optical semiconductor dice, such as light emitting diodes. These and other limitations may be exist with the conventional cleaving process.


Accordingly, it is desirable to provide an improved method for singulating dice.


BRIEF SUMMARY OF THE INVENTION

This invention provides techniques for manufacturing high brightness optical devices. More particularly, the method provides a processing method for removing slag material to enhance light output and efficiency of light emitting diodes, commonly termed LEDs.


The invention provides a manufacturing method for light emitting diode devices. The manufacturing method includes a technique for singulating dice from a substrate, e.g., a sapphire substrate or bulk gallium nitride. The method includes providing the substrate having a thickness of gallium and nitrogen containing material. Preferably, the substrate includes a plurality of die, with each die providing an LED device. The method also includes forming trenches by scanning a coherent beam of energy in a repetitive manner to respective portions of the surface. The scanned coherent beam, preferably derived from a laser, causes ablation of selected materials of the surface. The trenches extend from the surface of the substrate toward an opposing surface, without separating the die. The die may be held together by a thickness of adhesive material or a remaining thickness of the substrate. The trenches can be of desired shape, e.g., v-shaped.


The method causes formation of slag material along the trenches during their formation. The method also subjects the trenches and the slag to a chemical solution to selectively remove the slag without significantly changing the cross-section of the trenches. The chemical is preferably a potassium hydroxide solution, a potassium ferricyanide solution, or a hydrochloric acid solution, or combinations of them. Preferably, the chemical solution is a buffered potassium ferricyanide solution.


The method may further include increasing the temperature of the chemical solution from approximately 50° C. to a temperature below the boiling point of the solution. The die may then be broken apart. The method also includes mounting the substrates to a flexible adhesive thickness of material from which they are later removed.


In a specific embodiment, the invention provides a method which includes forming a plurality of trenches by scanning a coherent beam of energy in a repetitive manner across respective portions of the surface regions. Each of the trenches extends from the surface of the semiconductor substrate toward an opposing surface. Slag is formed along the trenches, but is later removed by subjecting the trenches and the slag to a chemical solution. The chemical solution comprises a potassium hydroxide solution, a potassium ferricyanide solution, or a hydrochloric acid solution. Upon completion each of the die is substantially free from slag.


The chemical solution has certain preferably characteristics. As an example, the potassium hydroxide solution consists of 45% potassium hydroxide by weight and 55% water by weight. The potassium ferricyanide solution consists of potassium hexacyanoferrate in a range of 30% to 40% by weight, potassium hydroxide in a range of 1% to 5% by weight and water in a range of 55%-69% by weight. The method also includes heating the hydrochloric acid solution to approximately 65° C. The hydrochloric acid solution consists of about 35% hydrochloric acid by weight and 65% water by weight.


The present method provides for a high efficiency bright light emitting diode device, e.g. with 100 lumens per Watt output. Preferably, the method maintains the shape of each of the trenches to within about 98% of their original shape even after removing the slag. That is, there is less than 2% and preferably less than 1% removal of the gallium and nitrogen containing material. Depending upon the embodiment, the present method achieves over a 100% increase in light output compared to no removal of the slag.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a cross-sectional view of a single light emitting diode;



FIG. 2 is a flow diagram showing the steps used to manufacture the light emitting diode shown in FIG. 1;



FIG. 3 is a cross-sectional view showing a substrate upon which the light emitting diode of FIG. 1 is produced;



FIG. 4 is a cross-sectional view showing the substrate in FIG. 3 with a p-type gallium nitride layer thereon;



FIG. 5 is a cross-sectional view of the substrate shown in FIG. 4 having a patterned photoresist layer thereon;



FIG. 6 is a cross-sectional view of the substrate shown in FIG. 4 having a plurality of metal layers thereon;



FIG. 7 is a cross-section view of the substrate shown in FIG. 6 after a lift-off process;



FIG. 8 is a cross-sectional view of the wafer shown in FIG. 6 with slag present;



FIG. 9 is a top view of the wafer shown in FIG. 8;



FIG. 10 is a cross-sectional view of the wafer shown in FIG. 8 after removal of slag; and



FIG. 11 is a diagram illustrating device performance.





DETAILED DESCRIPTION OF THE INVENTION


FIG. 1 shows a light emitting diode 10 on a substrate 12 of n-type gallium nitride GaN manufactured. An active layer 14 is formed upon substrate. Active layer 14 may comprise a single quantum well or multiple quantum wells, e.g. 2-10 quantum wells. A layer of p-type gallium nitride 16 is formed upon quantum wells 14, and a metal stack 18 is positioned upon layer 16. The stack is formed of three separate metal layers 20, 22 and 24. Layers 20 and 24 are platinum and layer 22 is silver.


Substrate 12 may have a large-surface orientation between ten degrees and 0.2 degree (or less) of (0 00 1), (0 00−1), {1−1 0 0}, {1 1−2 0}, {1−1 0.+−.1}, {1−1 0.+−.2}, {1−1 0.+−.3}, {2 0−2.+−.1}, or {1 1 −2.+−.2}. In one embodiment, the substrate has a semipolar large-surface orientation, designated by (hkil) Bravais-Miller indices, where i=−(h+k), 1 is nonzero and at least one of h and k are nonzero. The substrate preferably has a dislocation density below 104 cm2 and an optical absorption coefficient below 100 cm10−1 at wavelengths between about 465 nm and about 700 nm. The nitride base crystal has an optical absorption coefficient below 100 cm−1 at wavelengths between about 700 nm and about 6667 nm. The surface of substrate 12 has a dislocation density below 105 cm−2 and is substantially free of low-angle grain boundaries, or tilt boundaries, over a length scale of at least 3 millimeters. The substrate 12 may be doped with any suitable n-type dopants from group VI and group IV atoms, e.g., sulfur, selenium, tellurium, silicon, germanium. In the present embodiment, substrate 12 is doped with Si and O providing a dopant concentration of approximately of 3 E18 cm-3.


Active layer 14 preferably comprises InGaN wells and GaN barrier layers. In other embodiments, the well layers and barrier layers comprise AlwInxGa1-w-xN and AlyInzGa1-y-zN, respectively, where 0≦w,x,y,z,w+x,y+z≦1, where w<u,y and/or x>v,z so that the bandgap of the well layer(s) is less than that of the barrier layer(s) and the n-type substrate. The well layers and barrier layers each have a thickness between about 1 nm and about 20 nm. In another embodiment, active layer 14 comprises a double heterostructure, with an InGaN or AlwInxGa1-w-xN and AlyInzGa1-y-zN layer about 20 nm to about 500 nm thick surrounded by GaN or AlyInzGa1-y-zN layers, where w<u, y and/or x>v, z. The composition and structure of active layer 14 are chosen to provide light emission at a preselected wavelength. Active layer 14 may be left undoped (or unintentionally doped) or may be doped n-type or p-type. Active layer 14 is formed upon substrate 12 using standard processing techniques.


Layer 16 may be doped with any suitable p-type dopant, such as group II or IV atoms, e.g., magnesium, zinc, cadmium, silicon, and germanium. In the present example, layer is doped with magnesium to provide a dopant concentration of approximately 1e20 cm-3.


Referring to FIGS. 1, 2 and 3, during fabrication, light emitting diode 10 is fabricated concurrently with a plurality of other light emitting diodes on a common semiconductor wafer. Wafer 15 is doped with n-type dopants using known techniques, at step 100. At step 102, active layer 14 is formed upon wafer 15 using known techniques. Following formation of active layer 14, p-type gallium nitride layer 16 is formed thereupon, shown in FIG. 4, at step 104 of FIG. 2. At step 106 surface of layer is exposed to an acid-containing cleaning solution. The cleaning solution consists essentially of 15% of nitric acid by weight, 27% of hydrochloric acid by weight and 58% of water by weight. This provides cleaned surface 26.


Referring to both FIG. 2 and FIG. 5, at step 108 a patterned photo resist layer 28 is formed upon cleaned surface 26. Layer 28 has a shape of a battlement leaving portions 30 of cleaned surface 26, with segments 32 of photo resist material being present between adjacent portions 30. Following formation of patterned photo resist layer 28, wafer 15 regions 30 and segments 32 are exposed to a buffered oxide etch process, at step 110. To that end, wafer 15 dipped into a solution consisting essentially of 2% hydrofluoric acid by weight and 8.75% ammonium fluoride by weight, with the rest being water. At step 112, three metal layers are sequentially deposited upon portions and segments 32. Specifically, a platinum layer 34 is deposited, followed by deposition of a silver layer 36. Another platinum layer 38 is deposited upon silver layer 36.


Referring to FIG. 2, at step 114 a lift-off process is used to remove segments 32 and the portions of layers 34, 36 and 38 in superimposition therewith, leaving a plurality of spaced-apart metal stacks 40. As a result, regions 42, shown in FIG. 7, of exposed wafer 15 remain between the spaced-apart metal stacks 40.


Referring to both FIG. 2 and FIG. 8, at step 116, a trench 44 is formed in each regions 42, using desired techniques, such as laser etching using a coherent beam of energy in the ultra violet spectrum. It should be understood that a trench 44 is adjacent to each metal stack 40 and is positioned between each adjacent pair of metals stacks 40. As result, a plurality of trenches 44 are formed in wafer 15 to form a grid pattern, shown in FIG. 9. Referring again to FIG. 8, each trench 44 extends from surface 46 of wafer 15 toward an opposing surface 48. Each trench 44 includes a nadir 50 that is spaced-apart from surface 48, defining a bulwark 52. Bulwark 52 extends between nadir 50 and surface 48. After formation of trenches 44, bulwark 52 is cleaved using a three point bending technique to segment light emitting diode 10 from wafer 15, referred to as a die. Typically, all bulwarks 52 are subjected to the cleaving process concurrently so as to produce a plurality of dies. To assist in affixing the spatial location of each die after segmentation it is common to include a layer of flexible adhesive tape 58 upon surface 48.


A problem encountered with using laser etching is the creation of contaminants that remains on the light emitting diode 10, referred to as slag 45. Slag 45 includes gallium metal, GaNx and GaOx and causes reduced light output. Although slag 45 is shown primarily in trenches 44, in practice slag 45 may be present in virtually any region of wafer 15. To remove the slag, wafer 15 is subjected to a chemical solution at step 115. The chemic solution is selected from a set of solutions consisting essentially of a potassium hydroxide solution, a potassium ferricyanide solution and a hydrochloric acid solution. The potassium hydroxide solution consists of 45% of potassium hydroxide by weight and 55% water by weight. The potassium ferricyanide solution consists of potassium hexacyanoferrate in a range of 30% to 40% by weight, potassium hydroxide in a range of 1% to 5% by weight and water in a range of 55%-69% by weight; and the hydrochloric acid solution consists of 35% of hydrochloric acid by weight and 65% water by weight. It is desired that the hydrochloric acid solution is heated to approximately 65° C. in increase the efficacy of removing the slag. Although exposing wafer 15 to the chemical solution is done following formation of trenches 44, this may occur before or after cleaving of bulwark 52. As a result of exposure to chemical solution, slag 45 is removed from trenches 44 and the remaining portions of wafer. In another embodiment, it is possible to grow the quantum wells, scribe the wafer, dip the wafer in the chemicals to remove the slag, put down photo resist, deposit the metals, and then cleave the wafer.


Example

To prove the principles and operation of the invention, certain experiments were performed. These experiments are merely examples of the process. In this example, gallium and nitrogen containing substrates with LED devices were fabricated. The substrates were subjected to scribing using a laser process. Scribing occurred at an energy density of ablation, i.e. 0.075 W/um2. The laser process used a 6 um spot size 2.1 W laser with a 25 um pulse width set at 80 Khz. The ranges of laser output that the slag removal would work is from 400 nm to 200 nm with average power from 25 mw to 10 W. Preferably, the laser beam ablates a portion of the gallium and nitrogen containing material. After formation of the scribes and slag, removal occurred using potassium ferricyanide species in a solution including a potassium hexacyanoferrate in a range of 30% to 40% by weight, potassium hydroxide in a range of 1% to 5% by weight, and water in a range of 55%-69% by weight, which may be mixed and/or agitated, although is not required. The temperature of the solution ranges from about 60 to 75 degrees Celsius and is preferably about 65 degrees Celsius. Referring to FIG. 11, we achieved over a 100% improvement in relative light output once the slag was removed using the method of the invention. Also, the efficiency of conversion, commonly external quantum efficiency, exceeded 30% and is preferably about 40 to 50% and greater.


It should be understood that the description recited above is an example of the invention and that modifications and changes may be undertaken which are within the scope of the claimed invention. Therefore, the scope of the appended claims should be accorded the broadest interpretation so as to encompass all such modifications and similar arrangements, including a full scope of equivalents.

Claims
  • 1. A method of manufacturing high brightness LED devices, the method of manufacturing comprising: providing a gallium and nitrogen substrate having a surface with a plurality of light emitting diodes;treating the substrate to form a plurality of trenches among the light emitting diodes, the plurality of trenches extending from the surface toward an opposing surface, by scanning a coherent beam of energy onto the surface wherein the step of treating causes formation of slag along the plurality of trenches; andsubjecting the trenches and the slag to a chemical solution including potassium ferricyanide to substantially remove the slag without substantially changing the trenches,wherein the temperature of the chemical solution ranges from about 60 to 75 degrees Celsius, and the chemical solution comprises potassium hexacyanoferrate in a range of 30% to 40% by weight, potassium hydroxide in a range of 1% to 5% by weight, and water in a range of 55%-69% by weight.
  • 2. The method of claim 1 wherein the substrate comprises GaN, the slag is formed overlying each of the trenches, and at least some trenches have a protruding portion of slag, the slag having a lower density than a density of the substrate.
  • 3. The method of claim 1 further comprising separating the plurality of light emitting diodes from each other.
  • 4. The method of claim 3 wherein the step of separating comprises breaking the substrate apart using the trenches.
  • 5. The method of claim 4 further comprising; mounting the substrate to a flexible adhesive material prior to breaking the substrate apart, andremoving the light emitting diodes from the flexible adhesive material after breaking the substrate apart.
  • 6. The method of claim 1 further comprising heating the chemical solution to approximately 65° C.
  • 7. A method of separating individual semiconductor die having light emitting diodes formed on a surface of a substrate, wherein the substrate comprises gallium nitride, the method comprising: forming a plurality of trenches in the substrate by scanning the substrate with a coherent beam of energy, the plurality of trenches extending from the surface of the substrate toward an opposing surface, the step of forming the plurality of trenches also forming slag along the plurality of trenches;subjecting the substrate, including the trenches and the slag, to a chemical solution to selectively remove substantially all of the slag without substantially changing the trenches; andseparating the individual semiconductor die from each other,wherein the temperature of the chemical solution ranges from about 60 to 75 degrees Celsius, and the chemical solution consists of potassium hexacyanoferrate in a range of 30% to 40% by weight, potassium hydroxide in a range of 1% to 5% by weight and water in a range of 55%-69% by weight.
  • 8. The method as recited in claim 7 further comprising heating the chemical solution to approximately 65° C.
  • 9. The method as recited in claim 7 further comprising, after the step of forming the plurality of trenches, a step of mounting the substrate on a flexible adhesive layer.
  • 10. A method of manufacturing light emitting diode (LED) devices, the method comprising: providing a sapphire substrate including a layer of material, the layer containing gallium and nitrogen and having a plurality of LEDs thereon;forming a plurality of trenches in at least the layer of material by scanning the substrate with a coherent beam of energy, thereby causing ablation of surface regions of the substrate and formation of slag along the plurality of trenches;subjecting the substrate, including the trenches and the slag, to a chemical solution to selectively remove the slag without substantially changing the trenches; andseparating the plurality of LEDs from each other using the trenches,wherein the temperature of the chemical solution ranges from about 60 to 75 degrees Celsius, and the chemical solution comprises potassium hexacyanoferrate in a range of 30% to 40% by weight, potassium hydroxide in a range of 1% to 5% by weight and water in a range of 55%-69% by weight.
  • 11. The method as recited in claim 10 wherein: an adhesive tape is affixed to a bottom surface of the substrate; andthe LEDs are separated from each other by the trenches and then each LED is removed from the tape.
  • 12. The method as recited in claim 10 further comprising heating the chemical solution to above about 65° C.
  • 13. The method as recited in claim 10 wherein the plurality of trenches are formed using a pulsed laser.
US Referenced Citations (247)
Number Name Date Kind
4065688 Thornton Dec 1977 A
4870045 Gasper et al. Sep 1989 A
5331654 Jewell et al. Jul 1994 A
5607899 Yoshida et al. Mar 1997 A
5632812 Hirabayashi May 1997 A
5764674 Hibbs-Brenner et al. Jun 1998 A
5813753 Vriens et al. Sep 1998 A
6335771 Hiraishi Jan 2002 B1
6468882 Motoki et al. Oct 2002 B2
6498355 Harrah et al. Dec 2002 B1
6501154 Morita et al. Dec 2002 B2
6509651 Matsubara et al. Jan 2003 B1
6533874 Vaudo et al. Mar 2003 B1
6547249 Collins, III et al. Apr 2003 B2
6680959 Tanabe et al. Jan 2004 B2
6734461 Shiomi et al. May 2004 B1
6809781 Setlur et al. Oct 2004 B2
6855959 Yamaguchi et al. Feb 2005 B2
6956246 Epler et al. Oct 2005 B1
7009199 Hall Mar 2006 B2
7012279 Wierer, Jr. et al. Mar 2006 B2
7128849 Setlur et al. Oct 2006 B2
7208096 Akkipeddi et al. Apr 2007 B2
7285801 Eliashevich et al. Oct 2007 B2
7303630 Motoki et al. Dec 2007 B2
7341880 Erchak et al. Mar 2008 B2
7358542 Radkov et al. Apr 2008 B2
7358543 Chua et al. Apr 2008 B2
7390359 Miyanaga et al. Jun 2008 B2
7419281 Porchia et al. Sep 2008 B2
7470938 Lee et al. Dec 2008 B2
7483466 Uchida et al. Jan 2009 B2
7489441 Scheible et al. Feb 2009 B2
7491984 Koike et al. Feb 2009 B2
7535082 Nakayama et al. May 2009 B2
7550305 Yamagata et al. Jun 2009 B2
7598104 Teng et al. Oct 2009 B2
7622742 Kim et al. Nov 2009 B2
7718454 Nakamura et al. May 2010 B2
7733571 Li Jun 2010 B1
7786488 Nakayama et al. Aug 2010 B2
7816238 Osada et al. Oct 2010 B2
7858408 Mueller et al. Dec 2010 B2
7862761 Okushima et al. Jan 2011 B2
7871839 Lee et al. Jan 2011 B2
7884538 Mitsuishi et al. Feb 2011 B2
7897988 Chen et al. Mar 2011 B2
7923741 Zhai et al. Apr 2011 B1
8008165 Nakayama et al. Aug 2011 B2
8044412 Murphy et al. Oct 2011 B2
8142566 Kiyomi et al. Mar 2012 B2
8143148 Raring et al. Mar 2012 B1
8148180 Felker et al. Apr 2012 B2
8153475 Shum et al. Apr 2012 B1
8188504 Lee May 2012 B2
8198643 Lee et al. Jun 2012 B2
8207548 Nagai Jun 2012 B2
8207554 Shum Jun 2012 B2
8247886 Sharma et al. Aug 2012 B1
8247887 Raring et al. Aug 2012 B1
8252662 Poblenz et al. Aug 2012 B1
8268643 Matsumoto Sep 2012 B2
8293551 Sharma et al. Oct 2012 B2
8299473 D'Evelyn et al. Oct 2012 B1
8310143 Van De Ven et al. Nov 2012 B2
8313964 Sharma et al. Nov 2012 B2
8314429 Raring et al. Nov 2012 B1
8350273 Vielemeyer Jan 2013 B2
8389305 Felker et al. Mar 2013 B2
8431942 Butterworth Apr 2013 B2
8455894 D'Evelyn et al. Jun 2013 B1
8502465 Katona et al. Aug 2013 B2
8524578 Raring et al. Sep 2013 B1
8575728 Raring et al. Nov 2013 B1
8597967 Krames et al. Dec 2013 B1
8686431 Batres et al. Apr 2014 B2
20010009134 Kim et al. Jul 2001 A1
20010043042 Murazaki et al. Nov 2001 A1
20010055208 Kimura Dec 2001 A1
20020028564 Motoki et al. Mar 2002 A1
20020070416 Morse et al. Jun 2002 A1
20020096994 Iwafuchi et al. Jul 2002 A1
20020127824 Shelton et al. Sep 2002 A1
20020155691 Lee et al. Oct 2002 A1
20020182768 Morse et al. Dec 2002 A1
20030000453 Unno et al. Jan 2003 A1
20030001238 Ban Jan 2003 A1
20030020087 Goto et al. Jan 2003 A1
20030047076 Liu Mar 2003 A1
20030164507 Edmond et al. Sep 2003 A1
20030178617 Appenzeller et al. Sep 2003 A1
20040070004 Eliashevich et al. Apr 2004 A1
20040080256 Hampden-Smith et al. Apr 2004 A1
20040104391 Maeda et al. Jun 2004 A1
20040116033 Ouderkirk et al. Jun 2004 A1
20040124435 D'Evelyn et al. Jul 2004 A1
20040161222 Niida et al. Aug 2004 A1
20040207998 Suehiro et al. Oct 2004 A1
20040245543 Yoo Dec 2004 A1
20040251471 Dwilinski et al. Dec 2004 A1
20050087753 D'Evelyn et al. Apr 2005 A1
20050109240 Maeta et al. May 2005 A1
20050121679 Nagahama et al. Jun 2005 A1
20050167680 Shei et al. Aug 2005 A1
20050199899 Lin et al. Sep 2005 A1
20050214992 Chakraborty et al. Sep 2005 A1
20050224830 Blonder et al. Oct 2005 A1
20050263791 Yanagihara et al. Dec 2005 A1
20060038542 Park et al. Feb 2006 A1
20060060131 Atanackovic Mar 2006 A1
20060060872 Edmond et al. Mar 2006 A1
20060079082 Bruhns et al. Apr 2006 A1
20060097278 Goto et al. May 2006 A1
20060118799 D'Evelyn et al. Jun 2006 A1
20060163589 Fan et al. Jul 2006 A1
20060166390 Letertre et al. Jul 2006 A1
20060169993 Fan et al. Aug 2006 A1
20060186418 Edmond et al. Aug 2006 A1
20060189098 Edmond Aug 2006 A1
20060204865 Erchak et al. Sep 2006 A1
20060205199 Baker et al. Sep 2006 A1
20060214287 Ogihara et al. Sep 2006 A1
20060240585 Epler et al. Oct 2006 A1
20060255343 Ogihara et al. Nov 2006 A1
20060256482 Araki et al. Nov 2006 A1
20060272572 Uematsu et al. Dec 2006 A1
20060273339 Steigerwald et al. Dec 2006 A1
20060286695 Yanashima et al. Dec 2006 A1
20070045200 Moon et al. Mar 2007 A1
20070093073 Farrell et al. Apr 2007 A1
20070096239 Cao et al. May 2007 A1
20070105351 Motoki et al. May 2007 A1
20070114569 Wu et al. May 2007 A1
20070121690 Fujii et al. May 2007 A1
20070131967 Kawaguchi et al. Jun 2007 A1
20070202624 Yoon et al. Aug 2007 A1
20070210074 Maurer et al. Sep 2007 A1
20070228404 Tran et al. Oct 2007 A1
20070231978 Kanamoto et al. Oct 2007 A1
20070264733 Choi et al. Nov 2007 A1
20070280320 Feezell et al. Dec 2007 A1
20070290224 Ogawa Dec 2007 A1
20080023691 Jang et al. Jan 2008 A1
20080030976 Murazaki et al. Feb 2008 A1
20080054290 Shieh et al. Mar 2008 A1
20080073660 Ohno et al. Mar 2008 A1
20080081015 Sarayama et al. Apr 2008 A1
20080083741 Giddings et al. Apr 2008 A1
20080083929 Fan et al. Apr 2008 A1
20080087919 Tysoe et al. Apr 2008 A1
20080099777 Erchak et al. May 2008 A1
20080106212 Yen et al. May 2008 A1
20080121906 Yakushiji May 2008 A1
20080121913 McKenzie et al. May 2008 A1
20080121916 Teng et al. May 2008 A1
20080128752 Wu Jun 2008 A1
20080142781 Lee Jun 2008 A1
20080151543 Wang Jun 2008 A1
20080164489 Schmidt et al. Jul 2008 A1
20080164578 Tanikella et al. Jul 2008 A1
20080173884 Chitnis et al. Jul 2008 A1
20080179607 DenBaars et al. Jul 2008 A1
20080179610 Okamoto et al. Jul 2008 A1
20080194054 Lin et al. Aug 2008 A1
20080210958 Senda et al. Sep 2008 A1
20080211416 Negley et al. Sep 2008 A1
20080217745 Miyanaga et al. Sep 2008 A1
20080230765 Yoon et al. Sep 2008 A1
20080237569 Nago et al. Oct 2008 A1
20080261381 Akiyama et al. Oct 2008 A1
20080272463 Butcher et al. Nov 2008 A1
20080282978 Butcher et al. Nov 2008 A1
20080283851 Akita Nov 2008 A1
20080284346 Lee Nov 2008 A1
20080303033 Brandes Dec 2008 A1
20090065798 Masui et al. Mar 2009 A1
20090072252 Son et al. Mar 2009 A1
20090078955 Fan et al. Mar 2009 A1
20090081857 Hanser et al. Mar 2009 A1
20090086475 Caruso et al. Apr 2009 A1
20090140279 Zimmerman et al. Jun 2009 A1
20090146170 Zhong et al. Jun 2009 A1
20090194796 Hashimoto et al. Aug 2009 A1
20090206354 Kitano et al. Aug 2009 A1
20090227056 Kyono et al. Sep 2009 A1
20090250686 Sato et al. Oct 2009 A1
20090252191 Kubota et al. Oct 2009 A1
20090267098 Choi Oct 2009 A1
20090273005 Lin Nov 2009 A1
20090309110 Raring et al. Dec 2009 A1
20090315480 Yan et al. Dec 2009 A1
20090315965 Yamagata et al. Dec 2009 A1
20090321745 Kinoshita et al. Dec 2009 A1
20090321778 Chen et al. Dec 2009 A1
20100001300 Raring et al. Jan 2010 A1
20100006873 Raring et al. Jan 2010 A1
20100032691 Kim Feb 2010 A1
20100055819 Ohba et al. Mar 2010 A1
20100108985 Chung et al. May 2010 A1
20100109030 Krames et al. May 2010 A1
20100117101 Kim et al. May 2010 A1
20100117106 Trottier May 2010 A1
20100117118 Dabiran et al. May 2010 A1
20100148145 Ishibashi et al. Jun 2010 A1
20100155746 Ibbetson et al. Jun 2010 A1
20100195687 Okamoto et al. Aug 2010 A1
20100200837 Zimmerman et al. Aug 2010 A1
20100220262 DeMille et al. Sep 2010 A1
20100240158 Ter-Hovhannissian Sep 2010 A1
20100290208 Pickard Nov 2010 A1
20100295088 D'Evelyn et al. Nov 2010 A1
20100309943 Chakraborty et al. Dec 2010 A1
20100327291 Preble et al. Dec 2010 A1
20110017298 Lee Jan 2011 A1
20110056429 Raring et al. Mar 2011 A1
20110057205 Mueller et al. Mar 2011 A1
20110075694 Yoshizumi et al. Mar 2011 A1
20110101400 Chu et al. May 2011 A1
20110101414 Thompson et al. May 2011 A1
20110108081 Werthen et al. May 2011 A1
20110121331 Simonian et al. May 2011 A1
20110124139 Chang May 2011 A1
20110175200 Yoshida Jul 2011 A1
20110180781 Raring et al. Jul 2011 A1
20110182056 Trottier et al. Jul 2011 A1
20110186860 Enya et al. Aug 2011 A1
20110186874 Shum Aug 2011 A1
20110216795 Hsu et al. Sep 2011 A1
20110266552 Tu et al. Nov 2011 A1
20110279054 Katona et al. Nov 2011 A1
20110281422 Wang et al. Nov 2011 A1
20110309373 Sharma et al. Dec 2011 A1
20110315999 Sharma et al. Dec 2011 A1
20110317397 Trottier et al. Dec 2011 A1
20120007102 Feezell et al. Jan 2012 A1
20120104412 Zhong et al. May 2012 A1
20120178198 Raring et al. Jul 2012 A1
20120187412 D'Evelyn et al. Jul 2012 A1
20120199841 Batres et al. Aug 2012 A1
20120288974 Sharma et al. Nov 2012 A1
20130022758 Trottier Jan 2013 A1
20130026483 Sharma et al. Jan 2013 A1
20130044782 Raring Feb 2013 A1
20130112987 Fu et al. May 2013 A1
20130126902 Isozaki et al. May 2013 A1
20130234108 David et al. Sep 2013 A1
20140103356 Krames et al. Apr 2014 A1
Foreign Referenced Citations (12)
Number Date Country
2381490 Oct 2011 EP
06-334215 Dec 1994 JP
1997-082587 Mar 1997 JP
1999-340507 Dec 1999 JP
1999-340576 Dec 1999 JP
2001-177146 Jun 2001 JP
2003-031844 Jan 2003 JP
2007-110090 Apr 2007 JP
2008-084973 Apr 2008 JP
2008-172040 Jul 2008 JP
WO 2006062880 Jun 2006 WO
WO 2009001039 Dec 2008 WO
Non-Patent Literature Citations (99)
Entry
Notice of Allowance for U.S. Appl. No. 12/720,593 dated Jul. 11, 2012.
Office Action for U.S. Appl. No. 12/861,765 dated Jul. 2, 2012.
Office Action for U.S. Appl. No. 12/936,238 dated Aug. 30, 2012.
Notice of Allowance for U.S. Appl. No. 13/163,482 dated Jul. 31, 2012.
Notice of Allowance for U.S. Appl. No. 13/163,498 dated Jul. 23, 2012.
Office Action for U.S. Appl. No. 13/465,976 dated Aug. 16, 2012.
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.
Office Action for U.S. Appl. No. 12/749,476 dated Apr. 11, 2011.
Office Action for U.S. Appl. No. 12/749,476 dated Nov. 8, 2011.
Notice of Allowance for U.S. Appl. No. 12/749,476 dated May 4, 2012.
Notice of Allowance for U.S. Appl. No. 12/749,476 dated Jun. 26, 2012.
Office Action for U.S. Appl. No. 12/880,889 dated Sep. 19, 2012.
Notice of Allowance for U.S. Appl. No. 13/419,325 dated Dec. 4, 2012.
Aguilar, ‘Ohmic n-contacts to Gallium Nitride Light Emitting Diodes’, National Nanotechnologhy Infrastructure Network, 2007, p. 56-81.
Baker et al., ‘Characterization of Planar Semipolar Gallium Nitride Films on Spinel Substrates’, Japanese Journal of Applied Physics, vol. 44, No. 29, 2005, p. L920-L922.
Founta et al., ‘Anisotropic Morphology of Nonpolar a-Plane GaN Quantum Dots and Quantum Wells’, Journal of Applied Physics, vol. 102, vol. 7, 2007, p. 074304-1-074304-6.
Haskell et al., ‘Defect Reduction in (1100) m-plane gallium nitride via lateral epitaxial overgrowth by hydride vapor phase epitaxy’, Applied Physics Letters 86, 111917, 2005, p. 1-3.
Lu et al., ‘Etch-Pits of GaN Films with Different Etching Methods’, Journal of the Korean Physical Society, vol. 45, Dec. 2004, p. S673-S675.
Rickert et al., ‘n-GaN Surface Treatments for Metal Contacts Studied Via X-ray Photoemission Spectroscopy’, Applied Physics Letters, vol. 80, No. 2, Jan. 14, 2002, p. 204-206.
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, p. 57-60.
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.
Selvanathan et al., ‘Investigation of Surface Treatment Schemes on n-type GaN and Al 0.20Ga0.80N’, Journal of Vacuum Science and Technology B, vol. 23, No. 6, May 10, 2005, p. 2538-2544.
Semendy et al., ‘Observation and Study of Dislocation Etch Pits in Molecular Beam Epitaxy Grown Gallium Nitride with the use of Phosphoric Acid and Molten Potassium Hydroxide’, Army Research Laboratory, Jun. 2007, 18 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, 94th Edition, 2013-2014, p. 12-126-12-150.
Office Action for U.S. Appl. No. 12/491,169 dated Oct. 22, 2010 (9 pages).
Office Action for U.S. Application No. 12/491,169 dated May 11, 2011 (9 pages).
Office Action for U.S. Appl. No. 12/497,289 dated Feb. 2, 2012 (6 pages).
Notice of Allowance for U.S. Appl. No. 12/497,289 dated May 22, 2012 (7 pages).
Office Action for U.S. Appl. No. 12/785,953 dated Apr. 12, 2012 (11 pages).
Office Action for U.S. Appl. No. 12/785,953 dated Jan. 11, 2013 (14 pages).
Office Action for U.S. Appl. No. 12/785,953 dated Oct. 3, 2013 (10 pages).
Office Action for U.S. Appl. No. 12/880,803 dated Feb. 22, 2012 (8 pages).
Notice of Allowance for U.S. Appl. No. 12/880,803 dated Jul. 18, 2012 (5 pages).
Office Action for U.S. Appl. No. 12/995,946 dated Jan. 29, 2013 (25 pages).
Office Action for U.S. Appl. No. 12/995,946 dated Aug. 2, 2013 (15 pages).
Office Action for U.S. Appl. No. 13/019,897 dated Dec. 2, 2013 (17 pages).
Notice of Allowance for U.S. Appl. No. 13/281,221 dated Nov. 12, 2013 (10 pages).
Office Action for U.S. Appl. No. 13/328,978 dated Sep. 26, 2013 (25 pages).
Office Action for U.S. Appl. No. 13/548,635 dated Jun. 14, 2013 (5 pages).
Notice of Allowance for U.S. Appl. No. 13/548,635 dated Sep. 16, 2013 (6 pages).
Notice of Allowance for U.S. Appl. No. 13/548,770 dated Jun. 25, 2013 (6 pages).
Office Action for U.S. Appl. No. 13/629,366 dated Oct. 31, 2013 (7 pages).
Office Action for U.S. Appl. No. 13/723,968 dated Nov. 29, 2013 (23 pages).
Motoki et al., ‘Dislocation reduction in GaN crystal by advanced-DEEP’, Journal of Crystal Growth, vol. 305, Apr. 1, 2007, pp. 377-383.
Communication from the Japanese Patent Office re 2013515583 dated Feb. 27, 2014, 2 pages.
Office Action for U.S. Appl. No. 12/569,841 dated Feb. 14, 2014, 20 pages.
Office Action for U.S. Appl. No. 13/012,674 dated Jan. 17, 2014, 15 pages.
Office Action for U.S. Appl. No. 13/491,483 dated Jan. 16, 2014, 9 pages.
Office Action for U.S. Appl. No. 12/481,543 dated Jun. 27, 2011.
Office Action for U.S. Appl. No. 12/634,665 dated Mar. 12, 2012.
Office Action for U.S. Appl. No. 12/858,379 dated Apr. 14, 2011.
Notice of Allowance for U.S. Appl. No. 12/858,379 dated Dec. 6, 2011.
Office Action for U.S. Appl. No. 12/879,784 dated Jan. 25, 2012.
Notice of Allowance for U.S. Appl. No. 12/879,784 dated Apr. 3, 2012.
Office Action for U.S. Appl. No. 12/880,889 dated Feb. 27, 2012.
Office Action for U.S. Appl. No. 12/995,946 dated Mar. 28, 2012.
Office Action for U.S. Appl. No. 13/014,622 dated Nov. 28, 2011.
Office Action for U.S. Appl. No. 13/014,622 dated Apr. 30, 2012.
Office Action for U.S. Appl. No. 13/019,897 dated Mar. 30, 2012.
Kim et al., ‘High Brightness Light Emitting Diodes Using Dislocation-Free Indium Gallium Nitride/Gallium Nitride Multiquantum-Well Nanorod Arrays’, Nano Letters, vol. 4, No. 6, 2004, pp. 1059-1062.
Communication from the Korean Patent Office re 10-2012-7009980, dated Apr. 15, 2013.
Office Action for U.S. Appl. No. 12/569,841 dated Mar. 26, 2013.
Office Action for U.S. Appl. No. 12/749,466 dated Jul. 3, 2012.
Notice of Allowance for U.S. Appl. No. 12/936,238 dated Apr. 16, 2013.
Office Action for U.S. Appl. No. 13/019,897 dated Jan. 16, 2013.
Office Action for U.S. Appl. No. 13/328,978 dated May 15, 2013.
Office Action for U.S. Appl. No. 13/465,976 dated Dec. 20, 2012.
Notice of allowance for U.S. Appl. No. 13/184,160 (Dec. 12, 2011).
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, pp. 916-929.
Hanifin et al., ‘Photoreception for Circadian, Neuroendocrine, and Neurobehavioral Regulation’, Journal of Physiological Anthropology, vol. 26, 2007, pp. 87-94.
International Search Report & Written Opinion of PCT Application No. PCT/US2013/029453, dated Jul. 25, 2013, 11 pages total.
http://www.philipslumileds.com/products/luxeon-flash, ‘LUXEON Flash’, Philips Lumileds, Aug. 8, 2013, pp. 1-2.
Rea et al., ‘White Lighting’, COLOR Research and Application, vol. 38, No. 2, Sep. 3, 2011, pp. 82-92.
Office Action for U.S. Appl. No. 12/569,841 dated Aug. 13, 2013, 21 pages.
Office Action for U.S. Appl. No. 12/861,765 dated Sep. 17, 2013, 10 pages.
Office Action for U.S. Appl. No. 13/281,221 dated Jun. 21, 2013, 6 pages.
Notice of Allowance for U.S. Appl. No. 13/298,617 dated Sep. 13, 2013, 12 pages.
Iso et al., ‘High Brightness Blue InGaN/GaN Light Emitting Diode on Nonpolar m-Plane Bulk GaN Substrate,’ Japanese Journal of Applied Physics, 2007, vol. 46, No. 40, pp. L960-L962.
Office Action for U.S. Appl. No. 12/569,841 dated Dec. 23, 2011.
Office Action for U.S. Appl. No. 12/569,844 dated Oct. 12, 2012.
Notice of Allowance for U.S. Appl. No. 12/569,844 dated Mar. 7, 2013.
Notice of Allowance for U.S. Appl. No. 12/754,886 dated May 17, 2012.
Notice of Allowance for U.S. Appl. No. 12/754,886 dated Jun. 5, 2012.
Notice of Allowance for U.S. Appl. No. 12/754,886 dated Jun. 20, 2012.
Office Action for U.S. Appl. No. 12/861,765 dated Mar. 7, 2013.
Office Action for U.S. Appl. No. 12/936,238 dated Jan. 30, 2013.
Office Action for U.S. Appl. No. 13/025,833 dated Jul. 12, 2012.
Office Action for U.S. Appl. No. 13/179,346 dated Aug. 17, 2012.
Office Action for U.S. Appl. No. 13/179,346 dated Dec. 13, 2012.
Notice of Allowance for U.S. Appl. No. 13/419,325 dated Feb. 1, 2013.
Office Action for U.S. Appl. No. 13/425,354 dated Feb. 14, 2013.
Notice of Allowance for U.S. Appl. No. 12/785,953 dated Mar. 20, 2014 (8 pages).
Office Action for U.S. Appl. No. 12/861,765 dated Mar. 28, 2014 (12 pages).
Notice of Allowance for U.S. Appl. No. 13/012,674 dated Apr. 30, 2014 (8 pages).
Office Action for U.S. Appl. No. 13/019,897 dated Jun. 12, 2014 (8 pages).
Office Action for U.S. Appl. No. 13/357,578 dated May 13, 2014 (8 pages).
Office Action for U.S. Appl. No. 13/629,366 dated Apr. 18, 2014 (7 pages).
Office Action for U.S. Appl. No. 13/904,237 dated May 22, 2014 (13 pages).
Related Publications (1)
Number Date Country
20120135553 A1 May 2012 US