The invention is directed to optical devices. With the advent of semiconductor devices and applications thereof, GaN materials are being used for fabricating light emitting diodes (LEDs), lasers, and other types of devices. Typically, LEDs are formed over sapphire, silicon carbide, and on gallium nitride (GaN) substrates.
To form devices (e.g., LED or laser devices) over a GaN substrate, it is desirable to have a smooth surface. In the past, various processing techniques have been developed to achieve this goal. Unfortunately, conventional techniques have been inadequate.
Embodiments provided by the present disclosure are directed to optical devices. More specifically, embodiments of the invention provide a method for processing GaN based substrate material that can be used for manufacturing light-emitting diode, laser, and other types of devices. In various embodiments, a GaN substrate is exposed to gaseous species, which includes nitrogen and hydrogen material, at a high temperature for a predetermined period of time, and this process causes the surface of the GaN substrate to become smooth. Other processes, such as growing epitaxial layers over the surface of GaN substrate, are performed over the smooth surface of the GaN substrate.
In one embodiment, the invention provides a method for manufacturing semiconductor devices. The method includes providing a substrate. The substrate comprises gallium, and/or other Group III material, and nitrogen containing material. The substrate includes a top surface, which has scratches characterized by a depth of at least 8 nm. The method also includes providing a processing apparatus, which can be a chemical vapor deposition (CVD) apparatus. The CVD apparatus includes a chamber that has an initial temperature of between 10° C. and 60° C. The method additionally includes placing the substrate within the chamber of the CVD apparatus. The method also includes providing H2 and NH3 gaseous species within the chamber. Depending on the application, other types of gaseous species may be present within the chamber, such as N2, Ar, He, and others. Moreover, the method includes increasing the chamber temperature to a second temperature over a first time period. The second temperature is at least 900° C., but can also be greater than 1,000° C. The substrate may optionally be exposed to one or more of Group-III material during the second time period.
The method also includes subjecting the substrate to the second temperature for a second time period of about 5 minutes to 30 minutes. In addition, the method includes causing the top surface of the substrate to anneal at the second temperature. The plurality of scratches/trenches on the top surface of the substrate is characterized by a second scratch/trench depth of less than 2 nm as a result of the annealing. In various embodiments, at least a portion of the annealed substrate surface may be characterized by an RMS roughness of less than 0.05 nm over an area of 25 μm2. The terms scratches and trenches are used interchangeably herein to refer to substrate surface defects.
The method may include additional steps as well. For example, the method may include injecting NH3 into the chamber at a second temperature at a flow rate of 8 slpm. The method can also include forming epitaxial layers over the top surface. The method may additionally include doping the substrate with indium material over the annealed top surface. The top surface of the substrate may be polished before loading into the CVD chamber. Alternatively, the substrate could then be transferred to a second chamber (part of the same or different apparatus) for further thermal treatment and/or epitaxial growth/deposition.
During the first time period, as the temperature within the chamber increases, the top surface may have a temperature of about 100° C. less than the second temperature. The first time period can be about 12 minutes to 18 minutes. The second time period can be about 10 minutes.
The substrate, with a nitridation process performed over its surface, can be used to manufacture various types of devices, such as LED chips, power electronic devices, and others. To form LED chips using the substrate, the method may also include forming a rectifying device structure over the annealed surface. For example, the method can include forming a transistor device structure over the annealed surface. Prior to, or after the nitridation process, the substrate may optionally be patterned using conventional wet/dry etching techniques, or using metal/dielectric masks such as SiO2, SiN, or others.
According to another embodiment, the invention provides a method for manufacturing semiconductor devices. The method includes providing a substrate. The substrate comprises gallium and nitrogen containing material. The substrate has a top surface, which comprises a plurality of scratches characterized by a first scratch depth of at least 8 nm. The method also includes providing a chemical vapor deposition (CVD) apparatus. The CVD apparatus has a chamber, which has an initial temperature of between 10° C. and 60° C. The method also includes placing the substrate within the chamber of the CVD apparatus. Additionally, the method includes increasing the chamber temperature to a second temperature for a first period of time. The second temperature is at least 900° C. The method additionally includes subjecting the substrate to the second temperature for a second period of time about 5 minutes to 30 minutes and filling NH3 gaseous species into the chamber at a flow rate of at least 5 slpm. The method also includes causing the top surface of the substrate to anneal at the second temperature. The plurality of trenches on the top surface of the substrate is characterized by a second trench depth of less than 2 nm as a result of the annealing. The method also includes forming one or more epitaxial layers over the annealed surface.
In certain embodiments, method for manufacturing semiconductor devices are disclosed, the methods comprising: providing a substrate, the substrate comprising gallium and nitrogen containing material, the substrate having a top surface, the top surface comprising a plurality of scratches characterized by a first depth of at least 8 nm; providing a processing apparatus, the processing apparatus having a chamber, the chamber having an initial temperature of between 10 to 60° C., the apparatus being configured to cause the chamber to reach a temperature of at least 900° C. and change gas ambient within the chamber; placing the substrate within the chamber of the processing apparatus; providing H2 and NH3 gaseous species within the chamber; increasing the chamber temperature to a second temperature over a first time period, the second temperature being at least 900° C.; subjecting the substrate to the second temperature for a second time period of about 5 minutes to 30 minutes; and causing the top surface of the substrate to anneal at the second temperature, the plurality of scratches on the top surface of the substrate being characterized by a second depth of less than 2 nm as a result of the annealing, to provide an annealed substrate surface.
In certain embodiments, methods for manufacturing semiconductor devices are provided, the method comprising: providing a substrate, the substrate comprising gallium and nitrogen containing material, the substrate having a top surface, the top surface comprising a plurality of scratches characterized by a first depth of at least 8 nm; providing a processing apparatus, the processing apparatus having a chamber, the chamber having an initial temperature of between 10 to 60° C.; placing the substrate within the chamber of the processing apparatus; increasing the chamber temperature to a second temperature over a first time period, the second temperature being at least 1,300° C.; subjecting the substrate to the second temperature for a second time period of about 5 minutes to about 30 minutes and filling NH3 gaseous species into the chamber at a flow rate of at least 5 slpm; causing the top surface of the substrate to anneal at the second temperature, the plurality of scratches on the top surface of the substrate being characterized by a second depth of less than 2 nm as a result of the annealing to provide an annealed substrate surface; and forming one or more epitaxial layers over the anneal surface.
It is to be appreciated that embodiments of the invention provide numerous advantages compared to conventional techniques. Among other things, embodiments of the invention provide a process that smooth substrate surfaces, and/or reduces subsurface damage and extended defect density, thereby making the processed substrate better suited for forming various types of devices, such as LED chips, power electronics, etc.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments consistent with the present disclosure and, together with the description, serve to explain the principles of the disclosed embodiments. 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.
As mentioned above, GaN substrates with a smooth surface are desirable. Often, achieving a smooth surface prior to the growth of an active region is a requirement for achieving high performance devices, such as LEDs and laser diodes. A smooth growth surface can provide many benefits, such as:
1. Sharp interfaces between layers;
2. Minimize roughness-induced scattering, thereby resulting in higher carrier mobility;
3. Reduced point defect densities;
4. Uniform alloy, dopant composition indium incorporation across wafer; and/or
5. Prevents 3-D growth mode.
Achieving a smooth surface morphology is often difficult, especially for bulk GaN substrates. An in-situ surface treatment is often required to generate the step-structure, required for 2-D step-flow growth mode. The surface treatment is usually carried out in-situ and consists of ramping the temperature in a growth chamber in ammonia and hydrogen ambient, followed by nitridation of the GaN surface at an elevated temperature for a fixed amount of time. The optimum nitridation time, temperature, NH3 flow rate, H2 flow rate, etc. are determined empirically.
It is to be appreciated that depending on the application, the temperature and the temperature ramp time may be changed. For example, the MOCVD chamber can have a thermal couple temperature of greater than 1,000° C. In an embodiment, during the temperature ramp stage r, the NH3 flow is about 8 slpm and total H2 flow is about 31 slpm. Among other things, the NH3 gas preserves the surface of the substrate. Once the temperature at the MOCVD reaches the predetermined temperature, the substrate stays in the MOCVD chamber for a period of time (e.g., about 10 minutes) with the NH3 flow at about 8 slpm and total H2 flow at about 31 slpm, which substantially anneals the surface and enhances the smoothness and uniformity of the substrate surface. The amount of time for annealing the substrate surface varies, which can be from 5 minutes to 20 minutes. For example, the annealing process with the NH3 gaseous species can be referred as a nitridation process.
After the substrate bas been subject to both high temperature and NH3 and H2 within the MOCVD chamber, the surface of the substrate is smoothed and thus the substrate can be used for forming various types of devices. In an embodiment, an epitaxial film is formed over the smooth surface of the substrate. For example, the epitaxial film growth can be performed after the annealing process or after another ramp up in chamber temperature with NH3 material, as epitaxial film can be grown in high or low temperature.
The nitridation process illustrated in
According to an embodiment, the invention provides a method for manufacturing semiconductor devices. The method includes providing a substrate. The substrate comprises gallium and nitrogen containing material. The substrate includes a top surface, which comprises a plurality of scratches characterized by a first scratch depth of at least 8 nm. The method also includes providing a chemical vapor deposition (CVD) apparatus. The CVD apparatus includes a chamber that has an initial temperature of between 10° C. and 60° C. The method additionally includes placing the substrate within the chamber of the CVD apparatus. The method also includes providing H2 and NH3 gaseous species within the chamber. Moreover, the method includes increasing the chamber temperature to a second temperature over a first time period. The second temperature is at least 900° C., but can also be greater than 1,000° C. The substrate is exposed to one or more of Group-III material during the second time period.
The method also includes subjecting the substrate to the second temperature for a second time period of about 5 minutes to 30 minutes. In addition, the method includes causing the top surface of the substrate to anneal at the second temperature. The plurality of trenches on the top surface of the substrate is characterized by a second trench depth of less than 2 nm as a result of the annealing. In various embodiments, at least a portion of the annealed surface may be characterized by an RMS roughness of less than 0.05 nm over an area of 25 μm2.
The method above may include additional steps as well. For example, the method includes injecting NH3 into the chamber at the second temperature at a flow rate of 8 slpm. The method can also include forming one or more epitaxial layers over the top surface of the smooth substrate. The method may additionally include doping the smooth substrate with indium material over the annealed top surface. The top surface of the substrate may be polished before loading into the CVD chamber.
During the first time period as the temperature within the chamber increases, the top surface of the substrate may have a temperature of about 100° C. less than the second temperature. The first time period can be about 12 minutes to about 18 minutes. The second time period can be about 10 minutes.
The substrate, with the nitridation process performed over its surface, can be used to manufacture various types of devices, such as LED chips, power electronic devices, and others. To form LED chips using the smooth substrate, the method may also include forming a rectifying device structure over the annealed surface. For example, the method can include forming a transistor device structure over the annealed surface.
According to another embodiment, the invention provides a method for manufacturing semiconductor devices. The method includes providing a substrate. The substrate comprises gallium and nitrogen containing material. The substrate has a top surface, which comprises a plurality of scratches characterized by a first scratch depth of at least 8 nm. The method also includes providing a chemical vapor deposition (CVD) apparatus. The CVD apparatus has a chamber, which has an initial temperature of between 10° C. and 60° C. The method also includes placing the substrate within the chamber of the CVD apparatus. Additionally, the method includes increasing the chamber temperature to a second temperature over a first time period. The second temperature is at least 900° C. The method additionally includes subjecting the substrate to the second temperature for a second time period of about 5 minutes to 30 minutes and filling NH3 gaseous species into the chamber at a flow rate of at least 5 slpm. The method also includes causing the top surface of the substrate to anneal at the second temperature. The plurality of trenches on the top surface of the substrate is characterized by a second trench depth of less than 2 nm as a result of the annealing. The method also includes forming one or more epitaxial layers over the annealed surface.
While the above is a full description of the specific embodiments, various modifications, alternative constructions and equivalents may be used. Therefore, the above description and illustrations should not be taken as limiting the scope of the invention which is defined by the appended claims.
This application claims the benefit of U.S. Provisional Application No. 61/526,355, filed on Aug. 23, 2011, which is incorporated by reference in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
3647522 | Single | Mar 1972 | A |
4065688 | Thornton | Dec 1977 | A |
4341592 | Shortes et al. | Jul 1982 | A |
4860687 | Frijlink | Aug 1989 | A |
4911102 | Manabe et al. | Mar 1990 | A |
5331654 | Jewell et al. | Jul 1994 | A |
5334277 | Nakamura | Aug 1994 | A |
5527417 | Iida et al. | Jun 1996 | A |
5647945 | Matsuse et al. | Jul 1997 | A |
5663592 | Miyazawa et al. | Sep 1997 | A |
5698880 | Takahashi et al. | Dec 1997 | A |
5736753 | Ohno et al. | Apr 1998 | A |
5813753 | Vriens et al. | Sep 1998 | A |
5821555 | Saito et al. | Oct 1998 | A |
5864171 | Yamamoto et al. | Jan 1999 | A |
5888907 | Tomoyasu et al. | Mar 1999 | A |
5951923 | Horie et al. | Sep 1999 | A |
6123768 | Moustakas | Sep 2000 | A |
6153010 | Kiyoku et al. | Nov 2000 | A |
6239454 | Glew et al. | May 2001 | B1 |
6451157 | Hubacek | Sep 2002 | B1 |
6468882 | Motoki et al. | Oct 2002 | B2 |
6489636 | Goetz et al. | Dec 2002 | B1 |
6734461 | Shiomi et al. | May 2004 | B1 |
6755932 | Masuda et al. | Jun 2004 | B2 |
6814811 | Ose | Nov 2004 | B2 |
6833564 | Shen et al. | Dec 2004 | B2 |
6855959 | Yamaguchi et al. | Feb 2005 | B2 |
6858081 | Biwa et al. | Feb 2005 | B2 |
6875273 | Katamine et al. | Apr 2005 | B2 |
6920166 | Akasaka et al. | Jul 2005 | B2 |
7053413 | D'Evelyn et al. | May 2006 | B2 |
7135348 | Okuyama et al. | Nov 2006 | B2 |
7208096 | Akkipeddi et al. | Apr 2007 | B2 |
7312156 | Granneman et al. | Dec 2007 | B2 |
7348600 | Narukawa et al. | Mar 2008 | B2 |
7390359 | Miyanaga et al. | Jun 2008 | B2 |
7483466 | Uchida et al. | Jan 2009 | B2 |
7535082 | Nakayama et al. | May 2009 | B2 |
7550305 | Yamagata et al. | Jun 2009 | B2 |
7555025 | Yoshida | Jun 2009 | B2 |
7691658 | Kaeding et al. | Apr 2010 | B2 |
7709284 | Iza et al. | May 2010 | B2 |
7718454 | Nakamura et al. | May 2010 | B2 |
7727332 | Habel et al. | Jun 2010 | B2 |
7749326 | Kim et al. | Jul 2010 | B2 |
7786488 | Nakayama et al. | Aug 2010 | B2 |
7806078 | Yoshida | Oct 2010 | B2 |
7939354 | Kyono et al. | May 2011 | B2 |
7968864 | Akita et al. | Jun 2011 | B2 |
8008165 | Nakayama et al. | Aug 2011 | B2 |
8017932 | Okamoto et al. | Sep 2011 | B2 |
8153475 | Shum et al. | Apr 2012 | B1 |
8247887 | Raring et al. | Aug 2012 | B1 |
8268643 | Matsumoto | Sep 2012 | B2 |
8293551 | Sharma et al. | Oct 2012 | B2 |
8294179 | Raring | Oct 2012 | B1 |
8313964 | Sharma et al. | Nov 2012 | B2 |
8314429 | Raring et al. | Nov 2012 | B1 |
8389305 | Felker et al. | Mar 2013 | B2 |
8431942 | Butterworth | Apr 2013 | B2 |
8494017 | Sharma et al. | Jul 2013 | B2 |
8524578 | Raring et al. | Sep 2013 | B1 |
8597967 | Krames et al. | Dec 2013 | B1 |
8686431 | Batres et al. | Apr 2014 | B2 |
8749030 | Raring et al. | Jun 2014 | B2 |
8847249 | Raring et al. | Sep 2014 | B2 |
20010043042 | Murazaki et al. | Nov 2001 | A1 |
20020028564 | Motoki et al. | Mar 2002 | A1 |
20020085603 | Okumura | Jul 2002 | A1 |
20020127824 | Shelton et al. | Sep 2002 | A1 |
20030012243 | Okumura | Jan 2003 | A1 |
20030020087 | Goto et al. | Jan 2003 | A1 |
20030047076 | Liu | Mar 2003 | A1 |
20030080345 | Motoki et al. | May 2003 | A1 |
20030140846 | Biwa et al. | Jul 2003 | A1 |
20030200931 | Goodwin | Oct 2003 | A1 |
20040025787 | Selbrede et al. | Feb 2004 | A1 |
20040060518 | Nakamura et al. | Apr 2004 | A1 |
20040080256 | Hampden-Smith et al. | Apr 2004 | A1 |
20040089919 | Motoki et al. | May 2004 | A1 |
20040099213 | Adomaitis et al. | May 2004 | A1 |
20040116033 | Ouderkirk et al. | Jun 2004 | A1 |
20040146264 | Auner et al. | Jul 2004 | A1 |
20040151222 | Sekine | Aug 2004 | A1 |
20040175939 | Nakamura et al. | Sep 2004 | A1 |
20040233950 | Furukawa et al. | Nov 2004 | A1 |
20040245543 | Yoo | Dec 2004 | A1 |
20040247275 | Vakhshoori et al. | Dec 2004 | A1 |
20040262624 | Akita et al. | Dec 2004 | A1 |
20050001227 | Niki et al. | Jan 2005 | A1 |
20050012446 | Jermann et al. | Jan 2005 | A1 |
20050025205 | Ryowa et al. | Feb 2005 | A1 |
20050040384 | Tanaka et al. | Feb 2005 | A1 |
20050045894 | Okuyama et al. | Mar 2005 | A1 |
20050072986 | Sasaoka | Apr 2005 | A1 |
20050095861 | Ueno et al. | May 2005 | A1 |
20050139960 | Shibata | Jun 2005 | A1 |
20050214992 | Chakraborty et al. | Sep 2005 | A1 |
20050218413 | Matsumoto et al. | Oct 2005 | A1 |
20050218780 | Chen | Oct 2005 | A1 |
20050229855 | Raaijmakers | Oct 2005 | A1 |
20050245095 | Haskell et al. | Nov 2005 | A1 |
20060033009 | Kobayashi et al. | Feb 2006 | A1 |
20060060833 | Bruckner et al. | Mar 2006 | A1 |
20060066319 | Dallenbach et al. | Mar 2006 | A1 |
20060078022 | Kozaki et al. | Apr 2006 | A1 |
20060086319 | Kasai et al. | Apr 2006 | A1 |
20060086948 | Ohno et al. | Apr 2006 | A1 |
20060097278 | Goto et al. | May 2006 | A1 |
20060126688 | Kneissl | Jun 2006 | A1 |
20060144334 | Yim et al. | Jul 2006 | A1 |
20060186418 | Edmond et al. | Aug 2006 | A1 |
20060193359 | Kuramoto | Aug 2006 | A1 |
20060216416 | Sumakeris et al. | Sep 2006 | A1 |
20060240585 | Epler et al. | Oct 2006 | A1 |
20060272572 | Uematsu et al. | Dec 2006 | A1 |
20060286695 | Yanashima et al. | Dec 2006 | A1 |
20070045200 | Moon et al. | Mar 2007 | A1 |
20070081857 | Yoon | Apr 2007 | A1 |
20070093073 | Farrell et al. | Apr 2007 | A1 |
20070101932 | Schowalter et al. | May 2007 | A1 |
20070110112 | Sugiura | May 2007 | A1 |
20070111488 | Chakraborty et al. | May 2007 | A1 |
20070153866 | Shchegrov et al. | Jul 2007 | A1 |
20070163490 | Habel et al. | Jul 2007 | A1 |
20070184637 | Haskell et al. | Aug 2007 | A1 |
20070242716 | Samal et al. | Oct 2007 | A1 |
20070259464 | Bour et al. | Nov 2007 | A1 |
20070280320 | Feezell et al. | Dec 2007 | A1 |
20080001165 | Hashimoto et al. | Jan 2008 | A1 |
20080001174 | Shibata | Jan 2008 | A1 |
20080030976 | Murazaki et al. | Feb 2008 | A1 |
20080081015 | Sarayama et al. | Apr 2008 | A1 |
20080092812 | McDiarmid et al. | Apr 2008 | A1 |
20080095492 | Son et al. | Apr 2008 | A1 |
20080121916 | Teng et al. | May 2008 | A1 |
20080124817 | Bour et al. | May 2008 | A1 |
20080151543 | Wang | Jun 2008 | A1 |
20080173735 | Mitrovic et al. | Jul 2008 | A1 |
20080198881 | Farrell et al. | Aug 2008 | A1 |
20080232416 | Okamoto et al. | Sep 2008 | A1 |
20080251020 | Franken et al. | Oct 2008 | A1 |
20080257256 | Melnik et al. | Oct 2008 | A1 |
20080308815 | Kasai et al. | Dec 2008 | A1 |
20080315179 | Kim et al. | Dec 2008 | A1 |
20090021723 | De Lega | Jan 2009 | A1 |
20090066241 | Yokoyama | Mar 2009 | A1 |
20090080857 | St. John-Larkin | Mar 2009 | A1 |
20090081857 | Hanser et al. | Mar 2009 | A1 |
20090081867 | Taguchi et al. | Mar 2009 | A1 |
20090086475 | Caruso et al. | Apr 2009 | A1 |
20090141765 | Kohda et al. | Jun 2009 | A1 |
20090153752 | Silverstein | Jun 2009 | A1 |
20090155989 | Uematsu et al. | Jun 2009 | A1 |
20090159869 | Ponce et al. | Jun 2009 | A1 |
20090229519 | Saitoh | Sep 2009 | A1 |
20090309110 | Raring et al. | Dec 2009 | A1 |
20090309127 | Raring et al. | Dec 2009 | A1 |
20090315965 | Yamagata et al. | Dec 2009 | A1 |
20090316116 | Melville et al. | Dec 2009 | A1 |
20100006546 | Young et al. | Jan 2010 | A1 |
20100006876 | Moteki et al. | Jan 2010 | A1 |
20100031875 | D'Evelyn | Feb 2010 | A1 |
20100032644 | Akita et al. | Feb 2010 | A1 |
20100133656 | Hager et al. | Jun 2010 | A1 |
20100140745 | Khan et al. | Jun 2010 | A1 |
20100163887 | Kim et al. | Jul 2010 | A1 |
20100187540 | Ishibashi et al. | Jul 2010 | A1 |
20100195687 | Okamoto et al. | Aug 2010 | A1 |
20100213439 | Ueno | Aug 2010 | A1 |
20100220262 | DeMille et al. | Sep 2010 | A1 |
20100288190 | Zhang et al. | Nov 2010 | A1 |
20100295088 | D'Evelyn et al. | Nov 2010 | A1 |
20100309943 | Chakraborty et al. | Dec 2010 | A1 |
20100320462 | Koukitu et al. | Dec 2010 | A1 |
20100327291 | Preble et al. | Dec 2010 | A1 |
20110056429 | Raring et al. | Mar 2011 | A1 |
20110057205 | Mueller et al. | Mar 2011 | A1 |
20110075694 | Yoshizumi et al. | Mar 2011 | A1 |
20110129669 | Fujito et al. | Jun 2011 | A1 |
20110164637 | Yoshizumi et al. | Jul 2011 | A1 |
20110177631 | Gardner et al. | Jul 2011 | A1 |
20110203514 | Pimputkar et al. | Aug 2011 | A1 |
20110216795 | Hsu et al. | Sep 2011 | A1 |
20110247556 | Raring et al. | Oct 2011 | A1 |
20110315999 | Sharma et al. | Dec 2011 | A1 |
20120068188 | Feigelson | Mar 2012 | A1 |
20120135553 | Felker et al. | May 2012 | A1 |
20120187366 | Yoon | Jul 2012 | A1 |
20120314398 | Raring et al. | Dec 2012 | A1 |
20130016750 | Raring et al. | Jan 2013 | A1 |
20130022758 | Trottier | Jan 2013 | A1 |
20130044782 | Raring | Feb 2013 | A1 |
20130075770 | Chakraborty et al. | Mar 2013 | A1 |
20140103356 | Krames et al. | Apr 2014 | A1 |
20140346524 | Batres et al. | Nov 2014 | A1 |
Number | Date | Country |
---|---|---|
1783525 | Jun 2006 | CN |
1851942 | Oct 2006 | CN |
101944480 | Jan 2011 | CN |
03-287770 | Dec 1991 | JP |
06-508000 | Oct 1992 | JP |
11-340507 | Dec 1999 | JP |
2000-082676 | Mar 2000 | JP |
2000-223743 | Aug 2000 | JP |
2002-252371 | Sep 2002 | JP |
2003-060318 | Feb 2003 | JP |
2004-207519 | Jul 2004 | JP |
2004-536450 | Dec 2004 | JP |
2005-235908 | Sep 2005 | JP |
2005-244226 | Sep 2005 | JP |
2006-066869 | Mar 2006 | JP |
2006-093683 | Apr 2006 | JP |
2003-101081 | May 2006 | JP |
2006-156958 | Jun 2006 | JP |
2006-279025 | Oct 2006 | JP |
2006-308858 | Nov 2006 | JP |
2007-173467 | Jul 2007 | JP |
2007-537600 | Dec 2007 | JP |
2008-010749 | Jan 2008 | JP |
2008-091488 | Apr 2008 | JP |
2008-159606 | Jul 2008 | JP |
2009-038220 | Feb 2009 | JP |
2009-526379 | Jul 2009 | JP |
2002-084040 | Feb 2010 | JP |
2006-036561 | Jul 2010 | JP |
2010-219490 | Sep 2010 | JP |
2005-129896 | Nov 2010 | JP |
2006-257290 | Dec 2010 | JP |
2007-251214 | Apr 2011 | JP |
2007-188962 | Jul 2011 | JP |
2007-184352 | Nov 2011 | JP |
WO 2008041521 | Apr 2008 | WO |
WO 2011022699 | Feb 2011 | WO |
Entry |
---|
USPTO Office Action for U.S. Appl. No. 12/727,148 dated May 15, 2013. |
USPTO Office Action for U.S. Appl. No. 12/482,440 dated Feb. 23, 2011. |
USPTO Office Action for U.S. Appl. No. 12/482,440 dated Aug. 12, 2011. |
USPTO Office Action for U.S. Appl. No. 12/484,924 dated Apr. 14, 2011. |
USPTO Office Action for U.S. Appl. No. 12/484,924 dated Oct. 31, 2011. |
USPTO Office Action for U.S. Appl. No. 12/573,820 dated Mar. 2, 2011. |
USPTO Office Action for U.S. Appl. No. 12/573,820 dated Oct. 11, 2011. |
USPTO Office Action for U.S. Appl. No. 12/859,153 dated Feb. 26, 2013. |
Franssila, ‘Tools for CVD and Epitaxy’, Introduction to Microfabrication, 2004, pp. 329-336. |
USPTO Office Action for U.S. Appl. No. 12/859,153 dated Sep. 25, 2012. |
Communication from the Chinese Patent Office re 2010800458819 dated Feb. 27, 2014, 2 pages. |
USPTO Office Action for U.S. Appl. No. 12/482,440 dated Feb. 13, 2014, 7 pages. |
USPTO Office Action for U.S. Appl. No. 12/484,924 dated Dec. 18, 2013, 15 pages. |
USPTO Office Action for U.S. Appl. No. 12/573,820 dated Oct. 9, 2013, 28 pages. |
USPTO Office Action for U.S. Appl. No. 12/727,148 dated Nov. 21, 2013, 9 pages. |
USPTO Office Action for U.S. Appl. No. 13/046,565 dated Nov. 7, 2011, 16 pages. |
USPTO Office Action for U.S. Appl. No. 13/046,565 dated Feb. 2, 2012, 16 pages. |
USPTO Office Action for U.S. Appl. No. 13/046,565 dated Apr. 13, 2012, 39 pages. |
USPTO Office Action for U.S. Appl. No. 13/046,565 dated Jul. 19, 2012, 23 pages. |
USPTO Office Action for U.S. Appl. No. 13/621,485 dated Oct. 8, 2013, 6 pages. |
USPTO Notice of Allowance for U.S. Appl. No. 13/621,485 dated Feb. 4, 2014, 7 pages. |
Communication from the Japanese Patent Office re 2012-079345 dated Jul. 4, 2013, 15 pages. |
USPTO Office Action for U.S. Appl. No. 12/482,440 dated Aug. 15, 2013, 8 pages. |
USPTO Office Action for U.S. Appl. No. 12/859,153 dated Jun. 21, 2013, 24 pages. |
USPTO Office Action for U.S. Appl. No. 12/482,440 dated Feb. 13, 2014 (7 pages). |
USPTO Office Action for U.S. Appl. No. 12/484,924 dated Dec. 18, 2013 (15 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/484,924 dated May 29, 2014 (8 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/621,485 dated Feb. 4, 2014 (7 pages). |
Communication from the Japanese Patent Office re 2012-525744 dated Jun. 18, 2014 (14 pages). |
Communication from the Chinese Patent Office re 2011522148 dated Jul. 9, 2014 (7 pages). |
USPTO Office Action for U.S. Appl. No. 12/482,440 dated Sep. 11, 2014 (8 pages). |
USPTO Office Action for U.S. Appl. No. 12/727,148 dated Sep. 11, 2014 (11 pages). |
USPTO Office Action for U.S. Appl. No. 13/431,834 dated Sep. 3, 2014 (10 pages). |
Abare, ‘Cleaved and Etched Facet Nitride Laser Diodes’, IEEE Journal of Selected Topics in Quantum Electronics, vol. 4, No. 3, 1998, pp. 505-509. |
Aoki et al., ‘InGaAs/InGaAsP MQW Electroabsorption Modulator Integrated With a DFB Laser Fabricated by Band-Gap Energy Control Selective Area MOCVD’, IEEE Journal of Quantum Electronics, vol. 29, 1993, pp. 2088-2096. |
Asano et al., ‘100-mW Kink-Free Blue-Violet Laser Diodes With Low Aspect Ratio’, IEEE Journal of Quantum Electronics, vol. 39, No. 1, 2003, pp. 135-140. |
Bernardini et al., ‘Spontaneous Polarization and Piezoelectric Constants of III-V Nitrides’, Physical Review B, vol. 56, No. 16, 1997, pp. R10-024-R10-027. |
Caneau et al., ‘Studies on Selective OMVPE of (Ga,In)/(As,P)’, Journal of Crystal Growth, vol. 124, 1992, pp. 243-248. |
Chen et al., ‘Growth and Optical Properties of Highly Uniform and Periodic InGaN Nanostructures’, Advanced Materials, vol. 19, 2007, pp. 1707-1710. |
Founta et al., ‘Anisotropic Morphology of Nonpolar a-Plane GaN Quantum Dots and Quantum Wells’, Journal of Applied Physics, vol. 102, vol. 7, 2007, pp. 074304-1-074304-6. |
Funato et al., ‘Blue, Green, and Amber InGaN/GaN Light-Emitting Diodes on Semipolar (1122) GaN Bulk Substrates’, Japanese Journal of Applied Physics, vol. 45, No. 26, 2006, pp. L659-L662. |
Funato et al., ‘Monolithic Polychromatic Light-Emitting Diodes Based on InGaN Microfacet Quantum Wells Toward Tailor-Made Solid-State Lighting’, Applied Physics Express, vol. 1, 2008, pp. 011106-1-011106-3. |
Hiramatsu et al., ‘Selective Area Growth and Epitaxial Lateral Overgrowth of GaN by Metalorganic Vapor Phase Epitaxy and Hydride Vapor Phase Epitaxy’, Materials Science and Engineering, vol. B59, 1999, pp. 104-111. |
Khan, ‘Cleaved Cavity Optically Pumped InGaN—GaN Laser Grown on Spinel Substrates’, Applied Physics Letters, vol. 69, No. 16, 1996, pp. 2417-2420. |
Kuramoto et al., ‘Novel Ridge-Type InGaN Multiple-Quantum-Well Laser Diodes Fabricated by Selective Area Re-Growth on n-GaN Substrates’, Japanese Journal of Applied Physics, vol. 40, 2001, pp. L925-L927. |
Lin et al., ‘Influence of Separate Confinement Heterostructure Layer on Carrier Distribution in InGaAsP Laser Diodes With Nonidentical Multiple Quantum Wells’, Japanese Journal of Applied Physics, vol. 43, No. 10, 2004, pp. 7032-7035. |
Nakamura et al., ‘InGaN/Gan/AlGaN-Based Laser Diodes With Modulation-Doped Strained-Layer Superlattices Grown on an Epitaxially Laterally Overgrown GaN Substrate’, Applied Physics Letters, vol. 72, No. 2, 1998, pp. 211-213. |
Nam et al., ‘Lateral Epitaxial Overgrowth of GaN Films on SiO2 Areas Via Metalorganic Vapor Phase Epitaxy’, Journal of Electronic Materials, vol. 27, No. 4, 1998, pp. 233-237. |
Okamoto et al., ‘Pure Blue Laser Diodes Based on Nonpolar m-Plane Gallium Nitride With InGaN Waveguiding Layers’, Japanese Journal of Applied Physics, vol. 46, No. 35, 2007, pp. L820-L822. |
Okamoto et al., ‘High-Efficiency Continuous-Wave Operation of Blue-Green Laser Diodes Based on Nonpolar mPlane Gallium Nitride’, The Japan Society of Applied Physics, Applied Physics, Express 1, 2008, pp. 072201-1-072201-3. |
Okubo, ‘Nichia Develops Blue-Green Semiconductor Laser With 488 nm Wavelength’, http://techon.nikkeibp.co.jp/english/ NEWS—EN/20080122/146009, 2008. |
Park, ‘Crystal Orientation Effects on Electronic Properties of Wurtzite InGaN/GaN Quantum Wells’, Journal of Applied Physics, vol. 91, No. 12, 2002, pp. 9903-9908. |
International Search Report of PCT Application No. PCT/US2009/047107, dated Sep. 29, 2009, 14 pages total. |
International Search Report & Written Opinion of PCT Application No. PCT/US2010/030939, dated Jun. 16, 2010, 9 pages total. |
International Search Report & Written Opinion of PCT Application No. PCT/US2010/049172, dated Nov. 17, 2010, 7 pages total. |
International Search Report of PCT Application No. PCT/US2011/037792, dated Sep. 8, 2011, 2 pages total. |
Purvis, ‘Changing the Crystal Face of Gallium Nitride’, The Advance Semiconductor Magazine, vol. 18, No. 8, 2005, pp. 1-3. |
Romanov et al., ‘Strain-Induced Polarization in Wurtzite III-Nitride Semipolar Layers’, Journal of Applied Plysics, vol. 100, 2006, pp. 023522-1 through 023522-10. |
Sato et al., ‘High Power and High Efficiency Green Light Emitting Diode on Free-Standing Semipolar (1122) Bulk GaN Substrate’, Physica Status Solidi (RRL), vol. 1, No. 4, 2007, pp. 162-164. |
Schmidt et al., ‘Demonstration of Nonpolar m-Plane InGaN/GaN Laser Diodes’, Japanese Journal of Applied Physics, vol. 46, No. 9, 2007, pp. L190-L191. |
Schoedl, ‘Facet Degradation of GaN Heterostructure Laser Diodes’, Journal of Applied Physics, vol. 97, issue 12, 2006, pp. 123102-1-123102-8. |
Uchida et al., ‘Recent Progress in High-Power Blue-Violet Lasers’, IEEE Journal of Selected Topics in Quantum Electronics, vol. 9, No. 5, 2003, pp. 1252-1259. |
Waltereit et al., ‘Nitride Semiconductors Free of Electrostatic Fields for Efficient White Light-Emitting Diodes’, Letters to Nature: International Weekly Journal of Science, vol. 406, 2000, pp. 865-868. |
Yu et al., ‘Multiple Wavelength Emission From Semipolar InGaN/GaN Quantum Wells Selectively Grown by MOCVD’, Optical Society of America, 2007, pp. 1-2. |
USPTO Office Action for U.S. Appl. No. 12/491,169 dated Oct. 22, 2010 (9 pages). |
USPTO Office Action for U.S. Appl. No. 12/491,169 dated May 11, 2011 (9 pages). |
USPTO Office Action for U.S. Appl. No. 12/502,058 dated Dec. 8, 2010 (14 pages). |
USPTO Office Action for U.S. Appl. No. 12/502,058 dated Aug. 19, 2011 (12 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/502,058 dated Apr. 16, 2012 (10 pages). |
USPTO Office Action for U.S. Appl. No. 12/749,466 dated Jun. 29, 2011 (19 pages). |
USPTO Office Action for U.S. Appl. No. 12/749,466 dated Feb. 3, 2012 (14 pages). |
USPTO Office Action for U.S. Appl. No. 12/759,273 dated Nov. 21, 2011 (9 pages). |
USPTO Office Action for U.S. Appl. No. 12/762,269 dated Oct. 12, 2011 (11 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/762,269 dated Apr. 23, 2012 (8 pages). |
USPTO Office Action for U.S. Appl. No. 12/762,271 dated Dec. 23, 2011 (11 pages). |
USPTO Office Action for U.S. Appl. No. 12/762,271 dated Jun. 6, 2012 (12 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/762,278 dated Nov. 7, 2011 (10 pages). |
USPTO Office Action for U.S. Appl. No. 12/778,718 dated Nov. 25, 2011 (11 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/778,718 dated Apr. 3, 2012 (13 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/778,718 dated Jun. 13, 2012 (7 pages). |
USPTO Office Action for U.S. Appl. No. 12/789,303 dated Sep. 24, 2012 (19 pages). |
USPTO Office Action for U.S. Appl. No. 12/858,379 dated Apr. 14, 2011 (6 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/858,379 dated Dec. 6, 2011 (9 pages). |
USPTO Office Action for U.S. Appl. No. 12/868,441 dated Apr. 30, 2012 (11 pages). |
USPTO Office Action for U.S. Appl. No. 12/883,093 dated Mar. 13, 2012 (9 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/883,093 dated Nov. 21, 2012 (12 pages). |
USPTO Office Action for U.S. Appl. No. 12/883,652 dated Apr. 17, 2012 (7 pages). |
USPTO Office Action for U.S. Appl. No. 12/884,993 dated Mar. 16, 2012 (12 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 12/884,993 dated Nov. 26, 2012 (6 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/163,498 dated Jul. 23, 2012 (4 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/298,617 dated Sep. 13, 2013 (11 pages). |
USPTO Office Action for U.S. Appl. No. 13/304,182 dated May 9, 2014 (12 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/304,182 dated Aug. 27, 2014 (8 pages). |
USPTO Office Action for U.S. Appl. No. 13/354,639 dated Nov. 7, 2012 (11 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/354,639 dated Dec. 14, 2012 (8 pages). |
USPTO Office Action for U.S. Appl. No. 13/465,976 dated Aug. 16, 2012 (16 pages). |
USPTO Office Action for U.S. Appl. No. 13/465,976 dated Dec. 20, 2012 (16 pages). |
USPTO Office Action for U.S. Appl. No. 13/465,976 dated Aug. 25, 2014 (21 pages). |
USPTO Office Action for U.S. Appl. No. 13/491,483 dated Jan. 16, 2014 (9 pages). |
USPTO Office Action for U.S. Appl. No. 13/491,483 dated Jun. 27, 2014 (8 pages). |
USPTO Notice of Allowance for U.S. Appl. No. 13/491,483 dated Sep. 18, 2014 (7 pages). |
USPTO Office Action for U.S. Appl. No. 13/538,426 dated Nov. 21, 2014 (15 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. 14/181,386 dated Oct. 28, 2014 (10 pages). |
Number | Date | Country | |
---|---|---|---|
61526355 | Aug 2011 | US |