Method of making bulk InGaN substrates and devices thereon

Abstract
A relaxed epitaxial AlxInyGa(1-x-y)N layer on a substrate having a semipolar surface orientation includes a plurality of misfit dislocations in portions of the thickness of the epitaxial layer to reduce bi-axial strain to a relaxed state.
Description
CROSS-REFERENCES TO RELATED APPLICATIONS

This Non-Provisional patent application is based on and claims priority to Provisional Patent Application No. 61/392,565, titled METHOD OF MAKING BULK InGaN SUBSTRATES AND DEVICES THEREON, filed on Oct. 13, 2010. This provisional application is incorporated herein by reference for all purposes.


BACKGROUND OF THE INVENTION

The present invention relates generally to techniques using bulk gallium and nitrogen containing substrates. More particularly, the present invention provides a method and device using bulk gallium and nitrogen containing substrates configured in a semi-polar orientation. Merely by way of example, the invention has been applied to use bulk GaN substrates to form overlying epitaxial regions in a bi-axially relaxed state, but it would be recognized that the invention has a broader range of applicability.


Today's state-of-the-art visible-spectrum light-emitting diodes (LEDs) and laser diodes (LDs) in the ultraviolet to green (380-550 nm) regime are based on InGaN active layers grown pseudomorphic to wurtzite GaN. This is true whether the growth substrate is GaN itself, or a foreign substrate such as sapphire or SiC, since in the latter cases GaN-based nucleation layers are employed. To our knowledge, successful demonstration of InGaN-based nucleation layers has not been achieved, and may not be possible given the growth morphology evolution of low-temperature InGaN layers on foreign substrates. FIG. 1 illustrates the energy bandgap vs. basal-plane (a) lattice constant for a Wurtzite (Al, In, Ga)N system, with regions indicated for visible spectrum emission based on both strained-to-GaN and relaxed, InGaN. Reference number 110 represents the basal plane lattice constant for pseudomorphic InxGa1-xN/GAN, and 120 represents the basal plane lattice constant for relaxed InxGa1-xN.


The resulting built-in stress within the InGaN active layers can be problematic for achieving high quality material and good device operation as the InN mole fraction increases, a requirement for longer wavelength devices. For c-plane grown devices, increasing InN increases the built-in electric fields across the active layers due to spontaneous and piezoelectric polarization fields, reducing the overlap between electrons and holes and decreasing radiative efficiency. Moreover, there is evidence for material breakdown as the stress level becomes too high, resulting in so-called “phase separation,” beyond a critical limit of a certain InN mole fraction combined with a certain layer thickness. See, e.g. N. A. El-Masry, E. L. Piner, S. X. Liu, and S. M. Bedair, “Phase separation in InGaN grown by metalorganic chemical vapor deposition,” Appl. Phys. Lett., vol. 72, pp. 40-42, 1998. Such a limit is observed for InGaN layers of about 10% InN grown more than 0.2 um thick, for example, resulting in “black” or “grey” wafers.


Non-polar (1-100), (11-20), and semi-polar planes of GaN can address some of the problems above. In particular, for certain growth planes the combined spontaneous and piezoelectric polarization vector can be reduced to zero or near-zero, eliminating the electron-hole overlap problem prevalent in c-plane-based devices. Also, improved material quality with increased InN can be observed, such as demonstrated for semi-polar material which has resulted in continuous-wave (CW) true-green LDs for the first time. See, e.g. Y. Enya et al., “531 nm green lasing of InGaN based laser diodes on semi-polar {20-21} free-standing GaN substrates,” Appl. Phys. Express 2, 082101, 2009 and J. W. Raring et al., “High-power high-efficiency continuous-wave InGaN laser diodes in the violet, blue, and green wavelength regimes,” SPIE Photonics West 7602-43, 2010. The performance of longer-wavelength devices grown on these structures, however, still suffers considerably compared to that of shorter-wavelength counterparts. In addition, it is not clear that these growth plane orientations would eliminate the materials quality problems associated with strain. Recent characterization of semi-polar (Al,In,Ga)N heterostructures reveals the formation of a large density of misfit dislocations at heterointerfaces between AlGaN and GaN. See, for example, A. Tyagi et al., “Partial strain relaxation via misfit dislocation generation at heterointerfaces in (Al,In)GaN epitaxial layers grown on semipolar (11-22) GaN free standing substrates,” Appl. Phys. Lett. 95, 251905, 2009. These dislocations may act as non-radiative recombination centers as well as potential degradation mechanisms which may prevent long-life operation necessary for applications such as solid-state lighting. Finally, the best-reported external quantum efficiencies versus wavelength for LEDs show a strong reduction with increasing InN mole fraction, regardless of growth plane orientation, as illustrated by FIG. 2. FIG. 2 illustrates external quantum efficiency vs. peak emission wavelength for visible-spectrum light-emitting diodes (After S. Denbaars, DOE SSL Workshop presentation, February 2010). Reference number 210 is an efficiency curve for InxGa1-xN LEDs grown on a c-plane substrate. Reference number 220 is an efficiency curve representing (AlxGa1-x).52In.48P LEDs. Reference number 230 represents the efficiency of LEDs (nonpolar substrate), and reference numbers 232, 234, 236, and 238 each represents the efficiency of InxGa1-xN LEDs (semipolar substrates). Reference number 240 is an efficient curve for LEDs fabricated by UCSB.


BRIEF SUMMARY

According to the present invention, techniques related generally to using bulk gallium and nitrogen containing substrates are provided. More particularly, the present invention provides a method and device using bulk gallium and nitrogen containing substrates configured in a semi-polar orientation. Merely by way of example, the invention has been applied to use bulk GaN substrates to form overlying epitaxial regions in a bi-axially relaxed state, but it would be recognized that the invention has a broader range of applicability.


In this invention we activate the (0001)/1/3<11-20> slip planes in GaN by using semi-polar oriented material and controlled stress at heterointerfaces to form a relaxed InGaN layer which will become a seed for growth of a relaxed InGaN substrate or layer. In one embodiment, a GaN growth surface of a predetermined growth plane (other than c-plane) is provided. This may be accomplished by growing thick c-oriented boules of GaN by techniques such as hydride vapor-phase epitaxy (HVPE) and cutting these boules along predetermined orientations to provide a semi-polar GaN growth surfaces. Next, an InGaN seed layer of a specified InN mole fraction is grown upon the GaN layer by a desired technique such as metal-organic chemical vapor deposition (MOCVD), ammonothermal growth, molecular beam epitaxy (MBE), HVPE, or other methods. The predetermined growth plane combined with stress at the InGaN/GaN heterointerface results in the formation of a network of dislocations which allows the InGaN seed layer to relax. Continued growth of InGaN (by any one or a combination of the methods) results in a thicker, relaxed, InGaN layer with the dislocation density becoming reduced as layer thickness increases, due to annihilation of colliding dislocations. Once the total dislocation density is reduced to a level of about 108 cm−2, the InGaN layer is suitable to use for LED device fabrication. To reduce the dislocation density further, the total InGaN layer thickness is increased, and at a dislocation density level of 107 cm−2 or less, may be suitable for the growth of LD devices. The original GaN growth substrate may be removed at several points along the process flow.


In a specific embodiment, the present invention provides a method for forming at least one relaxed epitaxial AlxInyGa(1-x-y)N layer. The method includes providing a substrate having a semipolar surface orientation. In a preferred embodiment, the substrate may be GaN or other gallium and nitrogen containing material and the like. The method includes forming at least one epitaxial AlxInyGa(1-x-y)N layer having a thickness of at least 100 nanometers formed overlying at least a portion of the semipolar surface orientation such that a plurality of misfit dislocations are included in one or more portions of the thickness to reduce a bi-axial strain in the thickness to a relaxed state. The term “relaxed state” is ordinarily understood to mean substantially free from strain or in the preferred embodiment bi-axial strain. In a preferred embodiment, the forming comprising providing a predetermined thickness in the bi-axial strain and thereafter providing the plurality of misfit dislocations to reduce the bi-axial stain to or toward the relaxed state. The predetermined thickness is a critical thickness between a strained state and the relaxed state, which is substantially relaxed bi-axially. Of course, there can be other variations, modifications, and alternatives.


In an alternative specific embodiment, the present invention provides a device. The device includes a semi-polar bulk GaN substrate having a surface orientation within about 1 degree of one of (4 3 −7 1), (3 2 −5 1), (2 1 −3 1), (3 1 −4 2), (4 1 −5 3), (8 1 −9 8), and (3 0 −3 4), among others. The device includes at least one active layer comprising AlxInyGa1-x-yN, where 0≦x, y, x+y≦1. Preferably, the active layer has a thickness between about 1 nanometer and about 100 nanometer and a concentration of threading dislocations less than about 108 cm−2. In a specific embodiment, the device is selected from among a light emitting diode, a laser diode, a photodetector, an avalanche photodiode, a transistor, a rectifier, and a thyristor; one of a transistor, a rectifier, a Schottky rectifier, a thyristor, a p-i-n diode, a metal-semiconductor-metal diode, high-electron mobility transistor, a metal semiconductor field effect transistor, a metal oxide field effect transistor, a power metal oxide semiconductor field effect transistor, a power metal insulator semiconductor field effect transistor, a bipolar junction transistor, a metal insulator field effect transistor, a heterojunction bipolar transistor, a power insulated gate bipolar transistor, a power vertical junction field effect transistor, a cascode switch, an inner sub-band emitter, a quantum well infrared photodetector, a quantum dot infrared photodetector, a solar cell, and a diode for photoelectrochemical water splitting and hydrogen generation, among others.


In an alternative specific embodiment, the present invention provides a method for forming a relaxed epitaxial AlxInyGa(1-x-y)N layer. The method includes providing a substrate having an orientation within about 5 degrees of a c-plane and forming at least one epitaxial AlxInyGa(1-x-y)N layer with a thickness of at least 100 nanometers such that a plurality of misfit dislocations are included to reduce a bi-axial strain within the thickness or form a relaxed state.


One or more benefits may be achieved using one or more of the specific embodiments. As an example, the present device and method provides a substantially relaxed region for device fabrication using a gallium and nitrogen containing substrate. In a specific embodiment, the present method and device can be made using conventional techniques and is cost effective. In a preferred embodiment, dislocations are introduced into a thickness of the epitaxial layer to cause relaxation that is substantially biaxial. Depending upon the embodiment, one or more of these benefits can be achieved. These and other benefits are further described throughout the present specification and more particularly below.


The present invention achieves these benefits and others in the context of known process technology. However, a further understanding of the nature and advantages of the present invention may be realized by reference to the latter portions of the specification and attached drawings.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a diagram illustrating the relationship between energy bandgap and basal-plane lattice constant for strained InGaN and relaxed InGaN;



FIG. 2 is a diagram illustrating the relationship between external quantum efficiency and emission wavelength for LEDs as influenced by increasing InN mole fraction;



FIG. 3 is a diagram of an epitaxial layer on a substrate;



FIG. 4 is a plan-view diagram of surface projected onto c-plane;



FIG. 5 illustrates how photoresist may be developed by exposure to expanded laser beams incident at a preselected angle;



FIG. 6 illustrates how a mask with a predetermined lattice constant is formed by nanoimprint lithography;



FIG. 7 illustrates how a desired pattern is transferred from the photoresist to the substrate or epitaxial layer by etching;



FIG. 8 illustrates formation of an epitaxial layer on a patterned substrate; and



FIG. 9 illustrates how when an epitaxial layer is grown thick enough a substantial fraction of dislocations annihilate one another.





DETAILED DESCRIPTION

According to the present invention, techniques related generally to using bulk gallium and nitrogen containing substrates are provided. More particularly, the present invention provides a method and device using bulk gallium and nitrogen containing substrates configured in a semi-polar orientation. Merely by way of example, the invention has been applied to use bulk GaN substrates to form overlying epitaxial regions in a bi-axially relaxed state, but it would be recognized that the invention has a broader range of applicability.



FIG. 3 is a diagram of an epitaxial layer 303 on a substrate 301. In one embodiment, substrate 301 comprises bulk GaN. In other embodiments, substrate 301 comprises AlN, sapphire, silicon carbide, gallium arsenide, MgAl2O4 spinel, ZnO, BP, ScAlMgO4, YFeZnO4, MgO, Fe2NiO4, LiGa5O8, Na2MoO4, Na2WO4, In2CdO4, LiAlO2, LiGaO2, Ca8La2(PO4)6O2, or the like. Preferably, substrate 301 comprises bulk GaN with a surface dislocation density below about 107 cm−2. Epitaxial layer 303 may comprise AlxInyGa(1-x-y)N, where 0≦x, y≦1. In a preferred embodiment, at least one of x and y is between 0.01 and 0.50. The surface 305 of substrate 301 may have a semi-polar orientation, that is, may form an angle θ with respect to the (0001) c-plane in substrate 301 or with respect to the (0001) c-plane 307 in epitaxial layer 303 that is between 0 and 90 degrees. The crystallographic orientation of substrate surface 305 may be specified by Miller-Bravais indices (h k i l), where i=−(h+k), and where l and at least one of h and k are nonzero. The plane of the page in FIG. 3 is perpendicular to both surface 301 and c-plane 307.


Some semi-polar surface orientations, for example, {1 1 −2 2}, may be generated by tilting the [0 0 0 1] c axis toward an <1 1 −2 0> a axis. Other semi-polar surface orientations, for example, {1 0 −1 −1}, {1 0 −1 2}, {1 0 −1 3}, and {2 0 −2 1}, may be generated by tilting the [0 0 0 1] c axis toward an <1 0 −1 0> m axis. A number of authors have investigated epitaxial AlInGaN layers on bulk GaN substrates of such orientations. Still other semi-polar surface orientations may be generated by tilting the [0 0 0 1] c axis toward an axis intermediate in orientation intermediate between an a axis and an m axis. Such lower-symmetry orientations have not received much attention to date.



FIG. 4 is a schematic plan-view diagram of surface 305, projected onto c-plane 407. Surface 305 intersects c-plane 407 along line 409. Plane 411, projecting out of the page in FIG. 4, is perpendicular to both surface 305 and c-plane 407 and corresponds to the plane of the page in FIG. 3. Oriented within c-plane 407 lie the three a lattice vectors 413, 415, and 417. One of the a directions, for example, a3, may be closest in orientation to the normal of line 409, forming angle λ with respect to plane 411. In the case where the surface is generated by tilting toward an m axis, then two axes will be equidistant to plane 411 and λ will be 30 degrees.


In the nitrides, slip may occur relatively readily in the (0 0 0 1) basal plane, or c-plane, with a Burger's vector of ⅓ [1 1 −2 0] or a3. See A. Tyagi et al., “Partial strain relaxation via misfit dislocation generation at heterointerfaces in (Al,In)GaN epitaxial layers grown on semipolar (11-22) GaN free standing substrates,” Appl. Phys. Lett. 95, 251905, 2009 and Z. H. Wu et al., Appl. Phys. Lett. 96, 071909 (2010). Strain relaxation may occur by formation of misfit dislocations and slip motion of existing threading and/or misfit dislocations along (0 0 0 1) glide planes. Strain relaxation may also occur by formation of misfit dislocations with other orientations, dislocation climb, formation of stacking faults, cracking, roughening of the growth surface, and the like. In some or many cases the latter mechanisms for strain relaxation, however, may give rise to inferior crystallographic quality of the epitaxial layer. This invention seeks to maximize the extent of strain relaxation by generation of misfit dislocations.


Referring to FIG. 3 and FIG. 4, note that relaxation by introduction of a misfit dislocation along line 409 with Burger's vector a3 (along 413 in FIG. 4) may produce relaxation of magnitude b=a3 in c-plane 407, projection b cos θ cos λ, along surface 305 in the plane of the page of FIG. 3, and projection b sink along surface 305 out of the plane of the page of FIG. 3. In the case of tilt of the semi-polar surface from the c axis toward an a axis, λ=0 and generation of misfit dislocations in a single a direction may tend to produce relaxation in the direction along the c-axis projection but not the orthogonal direction, as observed by Tyagi et al. cited above. In the case of tilt of the semi-polar surface from the c axis toward an m axis, λ=30° and generation of misfit dislocations may be expected to occur with approximately equal probability along two a directions. For a given lattice mismatch, however, the magnitude of the stress along the a axes may be reduced from the case where slip only occurs along one a direction, and relaxation along two orthogonal surface directions may or may not be similar in magnitude.


Generation of an array of misfit dislocations, with a Burger's vector b equal to a, a line direction along {1 −1 0 0} and an average separation of d, may be expected to produce an in-plane (cf. FIG. 3) relaxation δ equal to (b/d) cos θ cos λ, and an out-of-plane relaxation δ of (b/d) sink. If the lattice mismatch is approximately equal in the directions parallel to the page and perpendicular to the page in FIG. 3, it may be desirable to have the in-plane and out-of-plane relaxations be approximately equal. If the lattice mismatch values in the two directions are not the same, it may be desirable to produce more relaxation in one direction than in the other, so as to produce an epitaxial layer that is fully relaxed in both directions.


Relaxation along surface 305 may be approximately equiaxial if cos θ=tan λ. This relation will hold for a single symmetry-equivalent set of tilt angles λ for a given off-c-axis tilt angle θ. For wurtzite structures with a near-ideal c/a ratios that are fairly similar between epitaxial layer and substrate, such as AlxInyGa(1-x-y)N on GaN, near-equiaxed relaxation may occur by generation of misfit dislocations for semi-polar surface orientations such as (4 3 −7 1), (3 2 −5 1), (2 1 −3 1), (3 1 −4 2), (4 1 −5 3), (8 1 −9 8), and (3 0 −3 4). These surfaces are tilted from the c axis by angles θ between about 85° and about 55° and have values of λ between about 5° and 30°.


As one example, consider growth of an epitaxial layer of In0.2Ga0.8N on the (2 1 −3 1) surface of bulk GaN. For this geometry θ is about 79° and λ is about 11°. Assuming Vegard's law, the lattice constants for the epitaxial layer are about 2% larger than those for GaN. Full relaxation of the strain may be achieved with misfit dislocations laterally separated by about 6 Å.


In one set of embodiments, a device is fabricated on a gallium-containing nitride substrate 305 whose semi-polar surface orientation is chosen such that cos θ=tan λ. In a specific embodiment, the orientation of gallium-containing nitride substrate 305 is selected to be within about 5 degrees, within about 2 degrees, within about 1 degree, or within about 0.5 degree from one of (4 3 −7 1), (3 2 −5 1), (2 1 −3 1), (3 1 −4 2), (4 1 −5 3), (8 1 −9 8), and (3 0 −3 4). One or more epitaxial and/or active layers may be deposited on the surface of substrate 305. In a preferred embodiment, the at least one epitaxial layer comprises AlxInyGa1-x-yN, where 0≦x, y, x+y≦1. An epitaxial or active layer may be subjected to a treatment, for example, a thermal treatment, that initiates the formation of misfit dislocations and avoids or minimizes the formation of threading dislocations in the active layer. The at least one active layer may have a value of y that is greater than 0.05, greater than 0.10, greater than 0.15, greater than 0.20, greater than 0.25, greater than 0.30, greater than 0.35, greater than 0.40, greater than 0.45, or greater than 0.50.


The active layer may be deposited by metalorganic chemical vapor deposition (MOCVD), by molecular beam epitaxy (MBE), by hydride vapor phase epitaxy (HVPE), or by other methods that are known in the art. The active layer may have a thickness between about 1 nanometer and about 100 nanometers. The active layer also may comprise a stack or superlattice of layers with alternating compositions. The active layer may have a concentration of threading dislocations less than about 107 cm−2, less than about 106 cm−2, less than about 105 cm−2, less than about 104 cm−2, or less than about 103 cm−2. At least one electrical contact is preferably deposited. In a preferred embodiment, the device is processed further to form a light emitting diode (LED) or a laser diode. In other embodiments, the device will be configured to be a photodetector, an avalanche photodiode, a transistor, a rectifier, and a thyristor; one of a transistor, a rectifier, a Schottky rectifier, a thyristor, a p-i-n diode, a metal-semiconductor-metal diode, high-electron mobility transistor, a metal semiconductor field effect transistor, a metal oxide field effect transistor, a power metal oxide semiconductor field effect transistor, a power metal insulator semiconductor field effect transistor, a bipolar junction transistor, a metal insulator field effect transistor, a heterojunction bipolar transistor, a power insulated gate bipolar transistor, a power vertical junction field effect transistor, a cascode switch, an inner sub-band emitter, a quantum well infrared photodetector, a quantum dot infrared photodetector, a solar cell, or a diode for photoelectrochemical water splitting and hydrogen generation.


In another set of embodiments, at least one epitaxial layer is grown on a substrate with a surface orientation within about 5 degrees of c-plane, and at least one of the substrate and at least one epitaxial layer are patterned to facilitate atom transport along glide planes to form misfit dislocations. If desired, a pattern, for example to provide stripes, bottom pillars, holes, or a grid, is formed on the substrate or on an epitaxial layer on the substrate by conventional photolithography.


In one set of embodiments, illustrated in FIGS. 5 and 6, a mask with a predetermined lattice constant may be formed by holographic photolithography. Photoresist 525 may be spin-coated on substrate or epitaxial layer 501 by methods that are known in the art. Suitable examples of the photoresist are Shipley SPR-3001, AZ-1518, and KMR-747.


Referring to FIG. 5, photoresist 525 may be developed by exposure to one or more expanded laser beams incident at a preselected angle. After an exposure at one position, the photoresist may be rotated by 90 degrees or by 60 degrees and/or by 120 degrees and exposed again. Upon washing with a suitable developer [for example, AZ-400K], a square or triangular mask with a predetermined periodicity is formed. The periodicity, or lattice constant of the pattern, may be controlled by changing the wavelength of the laser and the incidence angle during the exposure. In one specific embodiment, a He—Cd laser, operating at a wavelength of 325 nm, is used to expose the photoresist. In one specific embodiment, a single exposure is performed, forming a one-dimensional lattice of long stripes. In another specific embodiment, the photoresist is rotated by 60 degrees and/or 120 degrees and the wavelength and incident angle are left unchanged, so as to produce a triangular lattice. In another specific embodiment, the photoresist is rotated by 90 degrees and the wavelength and incident angle are left unchanged, so as to produce a square lattice. The pitch, or lattice constant, of the pattern may be chosen to be between about 10 nm and about 1000 nm for efficient formation of misfit dislocations.


In another embodiment, the mask with a predetermined lattice constant is formed by nanoimprint lithography, as shown in FIG. 6. To fabricate a nanoimprint master 627, a photoresist may be applied to a nanoimprint substrate. The nanoimprint substrate may constitute a silicon wafer with a 6-nm-thick SiO2 coating. In other embodiments, the nanoimprint substrate comprises at least one of quartz, fused silica, sapphire, silicon carbide, and diamond. A diamond substrate may be fabricated by chemical vapor deposition (CVD) or other suitable techniques. The photoresist may be exposed at two incident angles (or more), as described above, to form a patterned photoresist on the silicon wafer. In another embodiment, the photoresist for the nanoimprint master is patterned by electron-beam lithography, rather than by holographic lithography.


Two consecutive etching treatments, for example, by reactive ion etching, can be used to transfer the photonic crystal pattern from the photoresist to the SiO2 layer and then into the silicon wafer or other nanoimprint substrate. The final depth of the pattern in the silicon wafer or other nanoimprint substrate surface may be between about 100 nm and about 500 nm. In some embodiments, a different dry etch chemistry is selected to etch the nanoimprint substrate than is used to etch the photoresist and/or a SiO2 layer. Next, referring again to FIG. 6, a photoresist layer 625 may be deposited onto the substrate or epitaxial layer 601. One example of a suitable photoresist for this process is Nanonex NXR-1010. The photoresist is then imprinted by the nanoimprint master 627 at a predetermined temperature and pressure. In one embodiment, the temperature is about 130 degrees Celsius and the pressure is about 300 pounds per square inch. The thin layer of polymer left in the bottom of hollows produced by the imprinting process may then be etched away by performing reactive ion etching with O2.


Referring to FIG. 7, the desired pattern is then transferred from the photoresist to the substrate or epitaxial layer by etching. The etching conditions preferably are selected to maintain relatively straight sidewalls, with an angle θ with respect to the surface between about 60 degrees and about 90 degrees. In one implementation, the sidewall angle is between about 75 degrees and about 90 degrees. In some embodiments, the pattern is transferred by reactive ion etching with Cl2. The widths of the channels produced by etching may be between about 5 nm and about 1000 nm, and the depths between about 10 nm and about 100 microns, or between about 100 nm and about 10 microns.


In an alternative embodiment, the desired pattern is transferred to the substrate or epitaxial layer by masking. A suitable mask material, for example, silica (SiO2), silicon nitride (Si3N4), tungsten, gold, or the like, is deposited onto the patterned photoresist. The photoresist is then dissolved, removing excess masking material, except above the original openings in the patterned photoresist.


Following the patterning process, at least one epitaxial layer 803 is deposited on the patterned substrate or patterned epitaxial layer 801, as shown schematically in FIG. 8. During the initial stages of growth of epitaxial layer 803 the isolated nano- or micro-islands may be fully strained. As the thickness of epitaxial layer exceeds the Matthews Blakeslee critical thickness, at some point relaxation by formation and/or migration of misfit dislocations is expected to occur. In this case the (0 0 0 1) glide planes are parallel to the substrate-epitaxial-layer-interface, so dislocation motion and atom migration are expected to occur from the periphery of the nano- or micro-islands inward. As the thickness of epitaxial layer 803 continues to increase during deposition, the areas over the etched channels or masks begins to close off by lateral growth, and subsequent growth occurs on a coalesced layer. In some embodiments relaxation of the lattice mismatch strain goes to completion prior to coalescence.


In still another embodiment, the substrate is macroscopically patterned, with the pitch of the pattern between approximately 1 micron and about 1 millimeter. The pattern may comprise regions where the local crystallographic orientation is nonpolar or semipolar, rather than c-plane. Growth on these regions is expected to exhibit similar relaxation behavior as growth on a flat surface of the given orientation.


In one specific embodiment, a single epitaxial layer of the desired composition is grown directly on substrate 301. In another set of embodiments, a series of epitaxial layers of graded compositions, where each layer is much thicker than the Matthews-Blakeslee critical thickness, are grown on substrate 301. For example, a layer of In0.05Ga0.95N at least 1 micron thick, at least 10 microns thick, or at least 100 microns thick, may be deposited on the GaN substrate, followed by similarly-thick layers of In0.1Ga0.9N, In0.15Ga0.55N and In0.2Ga0.8N. The layer thicknesses may be similar to one another, or one or more layers may be substantially thicker than other layers.


In another embodiment, a series of epitaxial layers of graded compositions, where at least the first layer is thicker than the critical thickness and the indium fraction may decrease in sequential layers, are grown on substrate 301. For example, a layer of In0.3Ga0.7N at least 100 nanometers thick, at least 1 micron thick, at least 10 microns thick, or at least 100 microns thick, may be deposited on the GaN substrate, followed by layers of In0.25Ga0.75N, and In0.2Ga0.8N. The layer thicknesses may be similar to one another, or one or more layers may be substantially thicker than other layers. In a similar embodiment, the series of epitaxial layers of graded compositions may be grown without decreasing indium compositions in sequential layers, but instead sequential layers may have increasing or decreasing indium concentrations. For example, a layer of In0.3Ga0.7N at least 100 nanometers thick, at least 1 micron thick, at least 10 microns thick, or at least 100 microns thick, may be deposited on the GaN substrate, followed by layers of In0.1Ga0.9N, and of In0.2Ga0.8N. The layer thicknesses may be similar to one another, or one or more layers may be substantially thicker than other layers.


In still another set of embodiments, a graded AlxInyGa(1-x-y)N layer, with at least one stoichiometric coefficient x or y varying continuously as a function of vertical position within the layer, followed by an epitaxial layer of the desired, fixed composition, for example, In0.2Ga0.8N. The grading may be linear, nonlinear, quadratic, exponential, or the like. The grading may intentionally overshoot the final composition, followed by reverse grading to the final composition.


Generation of misfit dislocations may be facilitated by roughening the growth surface before deposition, for example, by deposition of nano-dots, islands, ion bombardment, ion implantation, or by light etching. Misfit dislocations may also preferentially be formed by modifying the lattice parameter of the substrate near the epitaxial by a process such as atomic diffusion, atomic doping, ion implantation, and/or mechanically straining the substrate. Generation of misfit dislocations may also be facilitated by deposition of a thin layer of AlxGa(1-x)N, for example, thinner than about 10 to 100 nanometers, followed by annealing to a temperature between about 1000 degrees and about 1400 degrees Celsius in an ammonia-rich atmosphere.


The relaxation and/or growth processes may also generate a significant concentration of threading dislocations. In preferred embodiments, the epitaxial layer is grown thick enough so that a substantial fraction of these dislocations annihilate one another by a similar mechanism as occurs on GaN, as illustrated in FIG. 9. For example, the total thickness of the epitaxial layer may be greater than 100 nanometers, greater than 1 micron, greater than 10 microns, greater than 100 microns, greater than 1 millimeter, or greater than 10 millimeters. The threading dislocation density in the resulting epitaxial layer may be less than 109 cm−2, less than 108 cm−2, less than 107 cm−2, or less than 106 cm−2.


In one specific embodiment, the epitaxial layer(s) is deposited by metalorganic chemical vapor deposition (MOCVD). In other embodiments, the epitaxial layer(s) is deposited by molecular beam epitaxy (MBE), by ammonothermal crystal growth, by liquid phase epitaxy (LPE) using a flux, or by a combination of these processes.


In further embodiments, an epitaxial layer is deposited by hydride vapor phase epitaxy or by halide vapor phase epitaxy. For example, a hydrogen halide HX (X═F, Cl, Br, or I) may be passed over one or more crucibles containing at least one of Al, Ga, and/or In, forming a group III metal halide, for example, MX or MX3 plus H2. In some embodiments, halogen X2 (X═F, Cl, Br, or I) is passed over one or more crucibles containing at least one of Al, Ga, and/or In, forming a group III metal halide, for example, MX or MX3. If the halogen is a solid or liquid at room temperature, halogen vapor may be formed by pre-heating, for example, using apparatus similar to that described by Suscavage and co-workers. See M. Suscavage et al., Phys. Stat. Solidi (a) 188, 477 (2001); V. Tassev et al., J. Crystal Growth 235, 140 (2002). The group III metal halide may then be mixed with a nitrogen source, such as ammonia (NH3), hydrazine (N2H4), or hydrazoic acid (HN3), and brought into contact with a substrate to deposit an AlxInyGa(1-x-y)N epitaxial layer on the substrate. Transport of the group III metal halide and/or the nitrogen source may be facilitated by the use of one or more carrier gases such as nitrogen, hydrogen, and argon, as is known in the art. The thermodynamics of formation of the group III metal bromides and iodides are generally not as favorable as those of the corresponding chlorides or fluorides, but they may decompose more readily on the substrate surface, which may be particularly useful for formation of indium-rich epitaxial layers. An example of a suitable apparatus is described in U.S. Pat. No. 6,955,719, which is hereby incorporated by reference in its entirety. The materials of construction of the apparatus may include silica, quartz, alumina, silicon carbide, boron nitride, pyrolytic boron nitride, or MCxNyOz, where 0≦x, y, z≦3 and M represents at least one metal selected from B, Al, Si, Ti, V, Cr, Y, Zr, Nb, Mo, La, Hf, Ta, or W.


In some embodiments, following deposition of an AlxInyGa(1-x-y)N epitaxial layer on one surface of the substrate, the substrate is turned over and a second AlxInyGa(1-x-y)N epitaxial layer is deposited on the back side of the substrate, as described in U.S. Patent Application Ser. Nos. 61/096,304, 61/148,361, 61/181,513 and 61/178,460, each of which is incorporated by reference in its entirety. Following the deposition of the backside AlxInyGa(1-x-y)N epitaxial layer, the substrate may be cut to a desired shape and a protective coating deposited on the edges. The substrate may then be used as a seed crystal for ammonothermal crystal growth of AlxInyGa(1-x-y)N epitaxial layers on both sides of the substrate simultaneously. The ammonothermal growth may be performed using techniques described by U.S. Patent Application Ser. No. 61/181,608 and/or by U.S. Pat. No. 7,642,122, each of which is hereby incorporated by reference in their entirety.


In one embodiment, the InGaN seed layer is grown out to provide a low dislocation density boule of InGaN, which is subsequently cut along predetermined orientations to provide an InGaN substrate of any preferred orientation. For example, InGaN substrates of orientations such as (0001), (1-100), (11-20), (10-11), (20-21), (30-34), (21-31), and other orientations are possible. Using the technique described, InGaN substrates with InN mole fractions from 0.5% to 50% may be provided, for example. These substrates can be used for growth of LED and LD devices at longer emission wavelengths with improved performance compared to devices grown on GaN. For example, high-performance green, yellow, amber, and even red LEDs and LDs can be provided. The amber and red devices based on InGaN can be expected to outperform the incumbent devices based on the cubic (Al,In,Ga)P material system due to the inherent bandstructure limitations of the latter such as low hetero-barrier potentials and presence of indirect bandgap minima close in energy to the direct bandgap, resulting in lower efficiency with increased InAlP mole fraction (for shorter wavelength emission) and poor thermal performance at nearly all emission wavelengths. See J. M. Phillips et al., “Research challenges to ultra-efficient inorganic solid-state lighting,” Laser & Photon. Rev. 1, 307-333, 2007. Examples of laser diode structures are described in U.S. Patent Application Ser. No. 61/181,608.


After growth, the AlxInyGa(1-x-y)N epitaxial layer may be removed from the substrate by methods that are known in the art to form a free-standing AlxInyGa(1-x-y)N layer, crystal, wafer, or boule. At least one surface may be lapped, polished, and/or chemical-mechanically polished. The free-standing AlxInyGa(1-x-y)N layer, crystal, wafer, or boule may have a semipolar orientation; a thickness of at least 100 nanometers, a threading dislocation density below about 109 cm−2, a stacking fault density less than about 103 cm−1, and a strain less than about 0.1%. The thickness may be at least 1 micron, at least 10 microns, at least 100 microns, or at least 1 millimeter. The dislocation density may be less than 108 cm−2, less than 107 cm−2, or less than 106 cm−2. The stacking fault density may be less than about 102 cm−1, less than about 10 cm−1, or less than about 1 cm−1. The strain may be less than about 0.01%, less than about 10−5, or less than about 10−6.


Active layer(s) may be deposited on the AlxInyGa(1-x-y)N epitaxial layer or on the free-standing AlxInyGa(1-x-y)N layer, crystal, wafer, or boule. The active layer may be incorporated into an optoelectronic or electronic devices such as at least one of a light emitting diode, a laser diode, a photodetector, an avalanche photodiode, a transistor, a rectifier, and a thyristor; one of a transistor, a rectifier, a Schottky rectifier, a thyristor, a p-i-n diode, a metal-semiconductor-metal diode, high-electron mobility transistor, a metal semiconductor field effect transistor, a metal oxide field effect transistor, a power metal oxide semiconductor field effect transistor, a power metal insulator semiconductor field effect transistor, a bipolar junction transistor, a metal insulator field effect transistor, a heterojunction bipolar transistor, a power insulated gate bipolar transistor, a power vertical junction field effect transistor, a cascode switch, an inner sub-band emitter, a quantum well infrared photodetector, a quantum dot infrared photodetector, a solar cell, and a diode for photoelectrochemical water splitting and hydrogen generation.


The InGaN substrates described herein allows the development of a new class of III-nitride visible-spectrum devices that will have superior performance throughout the visible spectrum and allows the realization of maximum efficiencies for systems employing these in applications, such as illumination and displays.


The embodiments described herein are examples of compositions, structures, systems and methods having elements corresponding to the elements of the invention recited in the claims. This written description enables one of ordinary skill in the art to make and use embodiments having alternative elements that likewise correspond to the elements of the invention recited in the claims. The scope thus includes compositions, structures, systems and methods that do not differ from the literal language of the claims, and further includes other compositions, structures, systems and methods with insubstantial differences from the literal language of the claims. While only certain features and embodiments have been illustrated and described herein, many modifications and changes may occur to one of ordinary skill in the relevant art. The appended claims are intended to cover all such modifications and changes.

Claims
  • 1. A method for forming a biaxially relaxed c-plane epitaxial AlxInyGa(1-x-y)N layer comprising: providing a substrate having a surface characterized by an orientation within 5 degrees of a c-plane;forming a pattern of channels in the substrate and isolated regions of the substrate defined by the channels, whereinthe channels are characterized by a sidewall angle with respect to the surface of the isolated regions between 60 degrees and 90 degrees and a pitch ranging from between 10 nm and 1000 nm; anda surface of the isolated regions is characterized by an orientation within 5 degrees of a c-plane;growing at least one AlxInyGa(1-x-y)N epitaxial layer on the isolated regions, comprising: growing a strained epitaxial AlxInyGa(1-x-y)N region on the isolated regions, wherein at least during initial stages of growth the strained epitaxial AlxInyGa(1-x-y)N region comprises a plurality of misfit dislocations; andincreasing a thickness of the at least one epitaxial AlxInyGa(1-x-y)N layer to cause the isolated regions to close off by lateral growth and to form a coalesced epitaxial AlxInyGa(1-x-y)N region, wherein the coalesced epitaxial AlxInyGa(1-x-y)N region is substantially free of misfit dislocations; andforming at least one biaxially relaxed c-plane epitaxial AlxInyGa(1-x-y)N layer overlying the coalesced epitaxial AlxInyGa(1-x-y)N region, whereina total thickness of the at least one epitaxial AlxInyGa(1-x-y)N layer is at least 100 nm; andthe biaxially relaxed c-plane epitaxial AlxInyGa(1-x-y)N layer is characterized by a biaxial strain less than 0.1% and a total threading dislocation density less than 108 cm−2.
  • 2. The method of claim 1 wherein at least one epitaxial AlxInyGa(1-x-y)N layer comprises at least two epitaxial AlxInyGa(1-x-y)N layers wherein at least one epitaxial AlxInyGa(1-x-y)N layer has a graded composition.
  • 3. The method of claim 1 further comprising subjecting the substrate to a roughening process before formation of the at least one epitaxial AlxInyGa(1-x-y)N epitaxial layer.
  • 4. The method of claim 1 further comprising forming a second epitaxial AlxInyGa(1-x-y)N layer on a back side of the substrate.
  • 5. The method of claim 1 wherein the total thickness of the at least one epitaxial AlxInyGa(1-x-y)N layer is greater than 1 micron.
  • 6. The method of claim 1 wherein the at least one epitaxial AlxInyGa(1-x-y)N layer comprises at least two epitaxial AlxInyGa(1-x-y)N layers characterized by a graded composition.
  • 7. The method of claim 1 wherein increasing the thickness of the at least one epitaxial AlxInyGa(1-x-y)N layer comprises: depositing AlxGa(1-x)N material at a first thickness of less than 100 nanometers;annealing the AlxGa(1-x)N material at a temperature ranging from between about 1000 degrees and 1400 degrees Celsius; anddepositing AlxGa(1-x)N material at a second thickness, wherein the a total thickness of the first thickness and the second thickness is greater than 100 nanometers.
  • 8. The method of claim 1 further comprising removing the substrate and the at least one epitaxial AlxInyGa(1-x-y)N layer to form a free-standing biaxially relaxed c-plane epitaxial AlxInyGa(1-x-y)N layer, crystal, wafer, or boule.
  • 9. The method of claim 1 further comprising fabricating a light emitting diode or a laser diode on at least a portion of the at least one epitaxial AlxInyGa(1-x-y)N layer.
  • 10. The method of claim 1, wherein the thickness of the at least one epitaxial AlxInyGa(1-x-y)N layer is greater than 10 microns.
  • 11. The method of claim 1, wherein the substrate comprises bulk gallium nitride.
  • 12. The method of claim 1, wherein the substrate comprises sapphire.
  • 13. The method of claim 1, further comprising depositing an additional epitaxial layer by hydride vapor phase epitaxy overlying the at least one AlxInyGa(1-x-y)N layer.
  • 14. The method of claim 1, wherein, at least a portion of the at least one epitaxial AlxInyGa(1-x-y)N layer proximate to the substrate is patterned; andat least a portion of the at least one epitaxial AlxInyGa(1-x-y)N layer distal to the substrate is coalesced or continuous and relaxed, having a strain, relative to fully-relaxed AlxInyGa(1-x-y)N, of less than 0.01%.
  • 15. The method of claim 1, wherein the at least one AlxInyGa(1-x-y)N layer comprises more than one epitaxial AlxInyGa(1-x-y)N layer, wherein at least a portion of a first epitaxial AlxInyGa(1-x-y)N layer overlying the substrate is patterned; andat least a portion of a second epitaxial AlxInyGa(1-x-y)N layer overlying the first epitaxial AlxInyGa(1-x-y)N layer is coalesced or continuous and relaxed, having a strain, relative to fully-relaxed AlxInyGa(1-x-y)N, of less than 0.01%.
  • 16. The method of claim 1, wherein at least one of x and y is between 0.01 and 0.50.
  • 17. A device comprising a biaxially relaxed epitaxial AlxInyGa(1-x-y)N layer formed by the method of claim 1, wherein the epitaxial AlxInyGa1-x-yN layer is characterized by: 0≦x, y, x+y≦1 and y>0.10;a surface orientation within 5 degrees of a c-plane;a thickness greater than 100 nanometer;a concentration of threading dislocations less than 108 cm−2; anda biaxial strain less than 0.1%.
  • 18. A device, comprising at least one layer comprising AlxInyGa1-x-yN, wherein the at least one layer is characterized by: 0≦x, y, x+y≦1 and y>0.10;a surface orientation within 5 degrees of a c-plane;a thickness greater than 100 nanometer;a concentration of threading dislocations less than 108 cm−2; anda biaxial strain less than 0.1%.
  • 19. The device of claim 18 wherein the device is selected from among a light emitting diode, a laser diode, a photodetector, an avalanche photodiode, a transistor, a rectifier, and a thyristor; one of a transistor, a rectifier, a Schottky rectifier, a thyristor, a p-i-n diode, a metal-semiconductor-metal diode, high-electron mobility transistor, a metal semiconductor field effect transistor, a metal oxide field effect transistor, a power metal oxide semiconductor field effect transistor, a power metal insulator semiconductor field effect transistor, a bipolar junction transistor, a metal insulator field effect transistor, a heterojunction bipolar transistor, a power insulated gate bipolar transistor, a power vertical junction field effect transistor, a cascode switch, an inner sub-band emitter, a quantum well infrared photodetector, a quantum dot infrared photodetector, a solar cell, and a diode for photoelectrochemical water splitting and hydrogen generation.
US Referenced Citations (259)
Number Name Date Kind
3245760 Sawyer Apr 1966 A
3303053 Strong et al. Feb 1967 A
3335084 Hall Aug 1967 A
4030966 Hornig et al. Jun 1977 A
4066868 Witkin et al. Jan 1978 A
4350560 Helgeland et al. Sep 1982 A
4430051 Von Platen Feb 1984 A
5098673 Engel et al. Mar 1992 A
5169486 Young et al. Dec 1992 A
5868837 DiSalvo et al. Feb 1999 A
6090202 Klipov Jul 2000 A
6129900 Satoh et al. Oct 2000 A
6152977 D'Evelyn Nov 2000 A
6273948 Porowski et al. Aug 2001 B1
6350191 D'Evelyn et al. Feb 2002 B1
6372002 D'Evelyn et al. Apr 2002 B1
6398867 D'Evelyn et al. Jun 2002 B1
6406540 Harris et al. Jun 2002 B1
6406776 D'Evelyn Jun 2002 B1
6455877 Ogawa et al. Sep 2002 B1
6475254 Saak et al. Nov 2002 B1
6528427 Chebi et al. Mar 2003 B2
6533874 Vaudo et al. Mar 2003 B1
6541115 Pender et al. Apr 2003 B2
6596040 Saak et al. Jul 2003 B2
6596079 Vaudo et al. Jul 2003 B1
6639925 Niwa et al. Oct 2003 B2
6656615 Dwilinski et al. Dec 2003 B2
6686608 Takahira Feb 2004 B1
6764297 Godwin et al. Jul 2004 B2
6765240 Tischler et al. Jul 2004 B2
6784463 Camras et al. Aug 2004 B2
6787814 Udagawa Sep 2004 B2
6806508 D'Evelyn et al. Oct 2004 B2
6858882 Tsuda et al. Feb 2005 B2
6861130 D'Evelyn et al. Mar 2005 B2
6887144 D'Evelyn et al. May 2005 B2
6936488 D'Evelyn et al. Aug 2005 B2
6955719 Dmitriev et al. Oct 2005 B2
7001577 Zimmerman et al. Feb 2006 B2
7009199 Hall et al. Mar 2006 B2
7009215 D'Evelyn et al. Mar 2006 B2
7012279 Wierer, Jr. et al. Mar 2006 B2
7026756 Shimizu et al. Apr 2006 B2
7033858 Chai et al. Apr 2006 B2
7053413 D'Evelyn et al. May 2006 B2
7063741 D'Evelyn et al. Jun 2006 B2
7067407 Kostamo et al. Jun 2006 B2
7078731 D'Evelyn et al. Jul 2006 B2
7098487 D'Evelyn et al. Aug 2006 B2
7101433 D'Evelyn et al. Sep 2006 B2
7102158 Tysoe et al. Sep 2006 B2
7105865 Nakahata et al. Sep 2006 B2
7112829 Picard et al. Sep 2006 B2
7119372 Stokes et al. Oct 2006 B2
7122827 Alizadeh et al. Oct 2006 B2
7125453 D'Evelyn et al. Oct 2006 B2
7160388 Dwilinski et al. Jan 2007 B2
7160531 Jacques et al. Jan 2007 B1
7170095 Vaudo et al. Jan 2007 B2
7175704 D'Evelyn et al. Feb 2007 B2
7198671 Ueda Apr 2007 B2
7208393 Haskell et al. Apr 2007 B2
7220658 Haskell et al. May 2007 B2
7252712 Dwilinski et al. Aug 2007 B2
7279040 Wang Oct 2007 B1
7285801 Eliashevich et al. Oct 2007 B2
7291544 D'Evelyn et al. Nov 2007 B2
7316746 D'Evelyn et al. Jan 2008 B2
7335262 Dwilinski et al. Feb 2008 B2
7338828 Imer et al. Mar 2008 B2
7364619 Dwilinski et al. Apr 2008 B2
7368015 D'Evelyn et al. May 2008 B2
7381391 Spencer et al. Jun 2008 B2
7420261 Dwilinski et al. Sep 2008 B2
7569206 Spencer et al. Aug 2009 B2
7572425 McNulty et al. Aug 2009 B2
7625446 D'Evelyn et al. Dec 2009 B2
7642122 Tysoe et al. Jan 2010 B2
7704324 D'Evelyn et al. Apr 2010 B2
7705276 Giddings et al. Apr 2010 B2
7759710 Chiu et al. Jul 2010 B1
7871839 Lee et al. Jan 2011 B2
7976630 Poblenz et al. Jul 2011 B2
8021481 D'Evelyn Sep 2011 B2
8048225 Poblenz et al. Nov 2011 B2
8097081 D'Evelyn Jan 2012 B2
8148801 D'Evelyn Apr 2012 B2
8188504 Lee May 2012 B2
8198643 Lee et al. Jun 2012 B2
8207548 Nagai Jun 2012 B2
8278656 Mattmann et al. Oct 2012 B2
8284810 Sharma et al. Oct 2012 B1
8299473 D'Evelyn et al. Oct 2012 B1
8303710 D'Evelyn Nov 2012 B2
8306081 Schmidt et al. Nov 2012 B1
8323405 D'Evelyn Dec 2012 B2
8329511 D'Evelyn Dec 2012 B2
8354679 D'Evelyn et al. Jan 2013 B1
8430958 D'Evelyn Apr 2013 B2
8435347 D'Evelyn et al. May 2013 B2
8444765 D'Evelyn May 2013 B2
8461071 D'Evelyn Jun 2013 B2
8465588 Poblenz et al. Jun 2013 B2
8482104 D'Evelyn et al. Jul 2013 B2
8492185 D'Evelyn et al. Jul 2013 B1
20010009134 Kim et al. Jul 2001 A1
20010011935 Lee et al. Aug 2001 A1
20010048114 Morita et al. Dec 2001 A1
20020070416 Morse et al. Jun 2002 A1
20020105986 Yamasaki Aug 2002 A1
20020182768 Morse et al. Dec 2002 A1
20020189532 Motoki et al. Dec 2002 A1
20030027014 Johnson et al. Feb 2003 A1
20030140845 D'Evelyn et al. Jul 2003 A1
20030145784 Thompson et al. Aug 2003 A1
20030164507 Edmond et al. Sep 2003 A1
20030183155 D'Evelyn et al. Oct 2003 A1
20030209191 Purdy Nov 2003 A1
20030232512 Dickinson et al. Dec 2003 A1
20040000266 D'Evelyn et al. Jan 2004 A1
20040023427 Chua et al. Feb 2004 A1
20040104391 Maeda et al. Jun 2004 A1
20040124435 D'Evelyn et al. Jul 2004 A1
20040161222 Niida et al. Aug 2004 A1
20040222357 King et al. Nov 2004 A1
20050087753 D'Evelyn et al. Apr 2005 A1
20050098095 D'Evelyn et al. May 2005 A1
20050109240 Maeta et al. May 2005 A1
20050121679 Nagahama et al. Jun 2005 A1
20050128469 Hall et al. Jun 2005 A1
20050152820 D'Evelyn et al. Jul 2005 A1
20050167680 Shei et al. Aug 2005 A1
20050191773 Suzuki et al. Sep 2005 A1
20050205215 Giddings et al. Sep 2005 A1
20050263791 Yanagihara et al. Dec 2005 A1
20060030738 Vanmaele et al. Feb 2006 A1
20060032428 Dwilinski et al. Feb 2006 A1
20060037529 D'Evelyn et al. Feb 2006 A1
20060037530 Dwilinski et al. Feb 2006 A1
20060038193 Wu et al. Feb 2006 A1
20060048699 D'Evelyn et al. Mar 2006 A1
20060096521 D'Evelyn et al. May 2006 A1
20060118799 D'Evelyn et al. Jun 2006 A1
20060124051 Yoshioka et al. Jun 2006 A1
20060163589 Fan et al. Jul 2006 A1
20060169993 Fan et al. Aug 2006 A1
20060177362 D'Evelyn et al. Aug 2006 A1
20060207497 D'Evelyn et al. Sep 2006 A1
20060213429 Motoki et al. Sep 2006 A1
20060214287 Ogihara et al. Sep 2006 A1
20060228870 Oshima Oct 2006 A1
20060246687 Kaiser et al. Nov 2006 A1
20060255343 Ogihara et al. Nov 2006 A1
20060288927 Chodelka et al. Dec 2006 A1
20060289386 Tysoe et al. Dec 2006 A1
20070015345 Baker et al. Jan 2007 A1
20070057337 Kano et al. Mar 2007 A1
20070077674 Okuyama 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
20070141819 Park et al. Jun 2007 A1
20070142204 Park et al. Jun 2007 A1
20070151509 Park et al. Jul 2007 A1
20070158785 D'Evelyn et al. Jul 2007 A1
20070164292 Okuyama Jul 2007 A1
20070166853 Guenther et al. Jul 2007 A1
20070178039 D'Evelyn et al. Aug 2007 A1
20070181056 D'Evelyn et al. Aug 2007 A1
20070190758 Kaeding et al. Aug 2007 A1
20070197004 Dadgar et al. Aug 2007 A1
20070210074 Maurer et al. Sep 2007 A1
20070215033 Imaeda et al. Sep 2007 A1
20070218703 Kaeding et al. Sep 2007 A1
20070228404 Tran et al. Oct 2007 A1
20070234946 Hashimoto et al. Oct 2007 A1
20070252164 Zhong et al. Nov 2007 A1
20070274359 Takeuchi et al. Nov 2007 A1
20070290224 Ogawa Dec 2007 A1
20080006831 Ng Jan 2008 A1
20080008855 D'Evelyn et al. Jan 2008 A1
20080023691 Jang et al. Jan 2008 A1
20080025360 Eichler et al. Jan 2008 A1
20080073660 Ohno et al. Mar 2008 A1
20080083741 Giddings et al. Apr 2008 A1
20080083929 Fan et al. Apr 2008 A1
20080083970 Kamber et al. Apr 2008 A1
20080087919 Tysoe et al. Apr 2008 A1
20080106212 Yen et al. May 2008 A1
20080121906 Yakushiji May 2008 A1
20080128752 Wu Jun 2008 A1
20080156254 Dwilinski et al. Jul 2008 A1
20080193363 Tsuji Aug 2008 A1
20080198881 Farrell et al. Aug 2008 A1
20080211416 Negley et al. Sep 2008 A1
20080230765 Yoon et al. Sep 2008 A1
20080272462 Shimamoto Nov 2008 A1
20080282978 Butcher et al. Nov 2008 A1
20080285609 Ohta et al. Nov 2008 A1
20080298409 Yamashita et al. Dec 2008 A1
20090078955 Fan et al. Mar 2009 A1
20090092536 Kawabata et al. Apr 2009 A1
20090146170 Zhong et al. Jun 2009 A1
20090218593 Kamikawa et al. Sep 2009 A1
20090250686 Sato et al. Oct 2009 A1
20090301387 D'Evelyn Dec 2009 A1
20090301388 D'Evelyn Dec 2009 A1
20090309105 Letts et al. Dec 2009 A1
20090309110 Raring et al. Dec 2009 A1
20090320744 D'Evelyn et al. Dec 2009 A1
20090320745 D'Evelyn et al. Dec 2009 A1
20100001300 Raring et al. Jan 2010 A1
20100003492 D'Evelyn Jan 2010 A1
20100003942 Ikeda et al. Jan 2010 A1
20100025656 Raring et al. Feb 2010 A1
20100031872 D'Evelyn Feb 2010 A1
20100031873 D'Evelyn Feb 2010 A1
20100031874 D'Evelyn Feb 2010 A1
20100031875 D'Evelyn Feb 2010 A1
20100031876 D'Evelyn Feb 2010 A1
20100032691 Kim Feb 2010 A1
20100075175 Poblenz et al. Mar 2010 A1
20100104495 Kawabata et al. Apr 2010 A1
20100108985 Chung et al. May 2010 A1
20100109030 Krames et al. May 2010 A1
20100109126 Arena May 2010 A1
20100117101 Kim et al. May 2010 A1
20100117118 Dabiran et al. May 2010 A1
20100147210 D'Evelyn Jun 2010 A1
20100151194 D'Evelyn Jun 2010 A1
20100189981 Poblenz et al. Jul 2010 A1
20100219505 D'Evelyn Sep 2010 A1
20100295088 D'Evelyn et al. Nov 2010 A1
20110017298 Lee Jan 2011 A1
20110062415 Ohta et al. Mar 2011 A1
20110064103 Ohta et al. Mar 2011 A1
20110100291 D'Evelyn May 2011 A1
20110108081 Werthen et al. May 2011 A1
20110121331 Simonian et al. May 2011 A1
20110175200 Yoshida Jul 2011 A1
20110183498 D'Evelyn Jul 2011 A1
20110220912 D'Evelyn Sep 2011 A1
20110256693 D'Evelyn et al. Oct 2011 A1
20110262773 Poblenz et al. Oct 2011 A1
20120000415 D'Evelyn et al. Jan 2012 A1
20120007102 Feezell et al. Jan 2012 A1
20120073494 D'Evelyn Mar 2012 A1
20120118223 D'Evelyn May 2012 A1
20120119218 Su May 2012 A1
20120137966 D'Evelyn et al. Jun 2012 A1
20120178215 D'Evelyn Jul 2012 A1
20120187412 D'Evelyn et al. Jul 2012 A1
20120199952 D'Evelyn et al. Aug 2012 A1
20130119401 D'Evelyn et al. May 2013 A1
20130251615 D'Evelyn et al. Sep 2013 A1
20130323490 D'Evelyn et al. Dec 2013 A1
Foreign Referenced Citations (8)
Number Date Country
101061570 Oct 2007 CN
2005-289797 Oct 2005 JP
2007-039321 Feb 2007 JP
WO 2005121415 Dec 2005 WO
2006057463 Jun 2006 WO
WO2007-004495 Jan 2007 WO
WO 2010068916 Jun 2010 WO
WO2012-016033 Feb 2012 WO
Non-Patent Literature Citations (146)
Entry
Anurag Tyagi et al “Partial strain relaxation via misfit dislocation generation at heterointerfaces in (Al,In)GaN epitaxial layers grown on semipolar (1122) GaN free standing substrate”, App. Phys. Lett 95. 251905 (2009).
Altoukhov et al., ‘High reflectivity airgap distributed Bragg reflectors realized by wet etching of AlInN sacrificial layers’, Applied Physics Letters, vol. 95, 2009, pp. 191102-1-191102-3.
Dorsaz et al., ‘Selective oxidation of AlInN Layers for current confinement in III-nitride devices’, Applied Physics Letters, vol. 87, 2005, pp. 072102-1 to 072102-3.
Ehrentraut et al., ‘The ammonothermal crystal growth of gallium nitride—A technique on the up rise’, Proceedings IEEE, 2010, 98(7), pp. 1316-1323.
Fang., ‘Deep centers in semi-insulating Fe-doped native GaN substrates grown by hydride vapour phase epitaxy’, Physica Status Solidi, vol. 5, No. 6, 2008, pp. 1508-1511.
Fujito et al., ‘Development of bulk GaN crystals and nonpolar/semipolar substrates by HVPE’, MRS Bulletin, 2009, 34, 5, pp. 313-317.
Gladkov et al., ‘Effect of Fe doping on optical properties of freestanding semi-insulating HVPE GaN:Fe’, Journal of Crystal Growth, vol. 312, 2010, pp. 1205-1209.
Grzegory, ‘High pressure growth of bulk GaN from Solutions in gallium’, Journal of Physics Condensed Matter, vol. 13, 2001, pp. 6875-6892.
Moutanabbir et al., ‘Bulk GaN Ion Cleaving’, Journal of Electronic Materials, vol. 39, No. 5, 2010, pp. 482-488.
Oshima et al., ‘Thermal and optical properties of bulk GaN crystals fabricated through hydride vapor phase epitaxy with void-assisted separation’, Journal of Applied Physics, vol. 98, 2005, pp. 103509-1-103509-4.
International Search Report of PCT Application No. PCT/US2009/67745, dated Feb. 5, 2010, 1 page total.
Porowski, ‘High Resistivity GaN Single Crystalline Substrates’, Acta Physica Polonica A, vol. 92, No. 5, 1997, pp. 958-962.
Porowski, ‘Near Defect Free GaN Substrates’, Journal of Nitride Semiconductor, 1999, pp. 1-11.
Sharma et al., ‘Vertically oriented GaN-based air-gap distributed Bragg reflector structure fabricated using band-gap-selective photoelectrochemical etching’, Applied Physics Letters, vol. 87, 2005, pp. 051107-1 to 051107-3.
USPTO Office Action for U.S. Appl. No. 12/133,365 dated May 13, 2013.
USPTO Office Action for U.S. Appl. No. 12/497,969 dated May 16, 2013.
USPTO Office Action for U.S. Appl. No. 12/636,683 dated Jun. 12, 2013.
USPTO Office Action for U.S. Appl. No. 12/891,668 dated Jan. 10, 2013.
USPTO Notice of Allowance for U.S. Appl. No. 12/891,668 dated Mar. 20, 2013.
USPTO Notice of Allowance for U.S. Appl. No. 13/175,739 dated Mar. 21, 2013.
USPTO Office Action for U.S. Appl. No. 13/346,507 dated Dec. 21, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 13/346,507 dated Apr. 22, 2013.
USPTO Notice of Allowance for U.S. Appl. No. 13/548,931 dated Jun. 3, 2013.
Byrappa et al., “Handbook of Hydrothermal Technology: A Technology for Crystal Growth and Materials Processing,” Noyes Publications, Park Ridge, New Jersey, 2001, pp. 94-96 and 152.
Callahan et al., “Synthesis and Growth of Gallium Nitride by the Chemical Vapor Reaction Process (CVRP),” 1999, MRS Internet Journal Nitride Semiconductor Research, vol. 4, Issue No. 10, pp. 1-6.
Chiang et al. “Luminescent Properties of Cerium-Activated Garnet Series Phosphor: Structure and Temperature Effects,” Journal of the Electrochemical Society 155:B517-B520 (2008).
Chiu et al. “Synthesis and Luminescence Properties of Intensely Red-Emitting M5Eu (WO4)4-x (MoO4)x (M=Li, Na, K) Phosphors,” Journal of the Electrochemical Society 15:J71-J78 (2008).
Ci et al. “Ca1-xMo1-yNbyO4:Eux3+: A novel red phosphor for white light emitting diodes,” Journal of Physics 152:670-674 (2008).
D'Evelyn et al., “Bulk GaN Crystal Growth by the High-Pressure Ammonothermal Method,” Journal of Crystal Growth, 2007, vol. 300, pp. 11-16.
Dwiliński et al, Ammono Method of BN, AIN, and GaN Synthesis and Crystal Growth,: Journal of Nitride Semiconductor Research, 1998, 3,25, MRS, Internet: http://nsr.mij.mrs.org.
Dwilinski et al., “Excellent Crystallinity of Truly Bulk Ammonothermal GaN,” Journal of Crystal Growth, 2008, vol. 310, pp. 3911-3916.
Ehrentraut et al., “Prospects for the Ammonothermal Growth of Large GaN Crystal,” Journal of Crystal Growth, 2007, vol. 305, pp. 304-310.
Farrell et al., “Continuous-wave Operation of AIGaN-cladding-free Nonpolar m-Plane InGaN/GaN Laser Diodes,” 2007, Japanese Journal of Applied Physics, vol. 46, No. 32, pp. L761-L763.
Feezell et al., “AIGaN-Cladding-Free Nonpolar InGaN/GaN Laser Diodes,” Japanese Journal of Applied Physics, vol. 46, No. 13, pp. L284-L286 (Mar. 2007).
Frayssinet et al., “Evidence of Free Carrier Concentration Gradient Along the c-axis for Undoped GaN Single Crystals,” Journal of Crystal Growth, 2001, vol. 230, pp. 442-447.
Fukuda et al. “Prospects for the ammonothermal growth of large GaN crystal,” Journal of Crystal Growth 305: 304-310 (Jul. 2007).
Happek “Development of Efficient UV-LED Phosphor Coatings for Energy Saving Solid State Lighting” University of Georgia (Jan. 2007).
Hashimoto et al. “Ammonothermal growth of bulk GaN,” Journal of Crystal Growth 310:3907-3910 (Aug. 2008).
Hashimoto et al. “A GaN bulk crystal wit improved structural quality grown by the ammonothermal method,” Nature Materials 6:568-671 (Jul. 2007).
Höppe et al. “Luminescence in Eu2+-doped Ba2Si5 N8: fluorescence, thernoliminescence, and upconversion”; Journal of Physics and Chemistry of Solids 61:2001-2006 (2000).
Iso et al., “High Brightness Blue InGaN/GaN Light Emitting Diode on Nonpolar m-plane Bulk GaN Substrate,” 2007, Japanese Journal of Applied Physics, vol. 46, No. 40, pp. L960-L962.
Kim et al, “Improved Electroluminescence on Nonpolar m-plane InGaN/GaN Qantum Well LEDs”, 2007, Physica Status Solidi (RRL), vol. 1, No. 3, pp. 125-127.
Kojima et al., “Stimulated Emission at 474 nm from an InGaN Laser Diode Structure Grown on a (1122) GaN Substrate ,” 2007, Applied Physics Letter, vol. 91, No. 25, pp. 251107-251107-3.
Kolis et al., “Crystal Growth of Gallium Nitride in Supercritical Ammonia,” Journal of Crystal Growth, 2001, vol. 222, pp. 431-434.
Kolis et al., “Materials Chemistry and Bulk Crystal Growth of Group III Nitrides in Supercritical Ammonia” Mat. Res. Soc. Symp. Proc., 1998, vol. 495, pp. 367-372.
Kubota et al., “Temperature Dependence of Polarized Photoluminescence from Nonpolar m-plane InGaN Multiple Quantum Wells for Blue Laser Diodes” 2008, Applied Physics Letter, vol. 92, pp. 011920-011920-3.
Li et al. “The effect of replacement of Sr by Ca on the structural and luminescence properties of the red-emitting Sr2Si5N8:Eu2+ LED conversion phosphor,” Journal of Solid State Chemistry 181:515-524 (2008).
Mirwald et al., “Low-Friction Cell for Piston-Cylinder High Pressure Apparatus,” Journal of Geophysical Research, 1975, vol. 80, No. 11, pp. 1519-1525.
Motoki et al. “Growth and Characterization of Freestanding GaN Substrates,” Journal of Crystal Growth, 2002, vol. 237-239, pp. 912-921.
Mueller-Mach et al. “Highly efficient all-nitride phosphor-converted white light emitting diode,” Physica Status Solidi (a) 202:1727-1732 (Jul. 2005).
Murota et al., “Solid State Light Source Fabricated with YAG:Ce Single Crystal,” 2002, Japanese Journal of Applied Physics, vol. 46, No. 41, Part 2, No. 8A, pp. L887-L888.
Okamoto et al., “Continuous-Wave Operation of m-Plane InGaN Multiple Quantum Well Laser Diodes,” 2007, Japanese Journal of Applied Physics, vol. 46, No. 9, pp. L187-L189.
Okamoto et al., “Pure Blue Laser Diodes Based on Nonpolar m-Plane Gallium Nitride with InGaN Waveguiding Layers,” 2007, Japanese Journal of Applied Physics, vol. 46, No. 35, pp. L820-L822.
Oshima et al., “Thermal and Optical Properties of Bulk GaN Crystals Fabricated Through Hydride Vapor Phase Epitaxy with Void-Assisted Separation,” 2005, Journal of Applied Physics, vol. 98, pp. 103509-1-103509-3.
Peters, “Ammonothermal Synthesis of Aluminium Nitride,” Journal of Crystal Growth, 1999, vol. 4, pp. 411-418.
Sarva, et al. “Dynamic compressive strength of silicon carbide under uniaxial compression,” Mat. Sci. & Eng. A 317,140 (2001).
Sato et al., “High Power and High Efficiency Green Light Emitting Diode on free-Standing Semipolar (1122) Bulk GaN Substrate,” 2007.Physica Status Solidi (RRL), vol. 1, pp. 162-164.
Sato et al., “Optical Properties of Yellow Light-Emitting-Diodes Grown on Semipolar (1122) Bulk GaN Substrate,” 2008, Applied Physics Letter, vol. 92, No. 22, pp. 221110-1-221110-3.
Schmidt et al., “Demonstration of Nonpolar m-Plane InGaN/GaN Laser Diodes ,” 2007, Japanese Journal of Applied Physics, vol. 46, No. 9, L190-L191.
Setlur et al. “Crystal chemistry and luminescence of Ce3+-doped (Lu2CaMg2)-Ca-2(Si, Ge)O12 and its use in LED based lighting,” Chemistry of Materials 18: 3314-3322 (2006).
Sizov et al., “500-nm Optical Gain Anisotropy of Semipolar (1122) InGaN Quantum Wells,” 2009, Applied Physics Express, vol. 2, pp. 071001-1-071001-3.
Tsuda et al., “Blue Laser Diodes Fabricated on m-Plane GaN Substrates,” 2008, Applied Physics Express, vol. 1, pp. 011104-011104-03.
Tyagi et al., “Semipolar (1011) InGaN/GaN Laser Diodes on Bulk GaN Substrates,” 2007, Japanese Journal of Applied Physics, vol. 46, No. 19, pp. L444-L445.
Wang et al. “Ammonothermal growth of GaN crystals in alkaline solutions,” Journal of crystal Growth 287:376-380 (Jan. 2006).
Wang et al. “New red Y0.85Bi0.1Eu0.05V1-yMyO4 (M=Nb, P) phosphors for light-emitting diodes,” Physica B: Condensed Matter 403:2071-2075 (Jun. 2008).
Wang et al., “Ammonothermal Synthesis of III-Nitride Crystals,” Crystal Growth & Design, 2006, vol. 6, Issue No. 6, pp. 1227-1246.
Wang et al., “Synthesis of Dense Polycrystaline GaN of High Purity by the Chemical Vapor Reaction Process,” Journal of Crystal Growth, 2006, vol. 286, pp. 50-54.
Yamamoto “White LED phosphors: the next step,” Proceeding of . SPIE (2010).
Yang et al. “Preparation and luminescence properties of LED conversion novel phosphors SrZnO2:Sm,” Materials Letters 62:907-910 (Mar. 2008).
Zhong et al., “Demonstration of High Power Blue-Green Light Emitting Diode on Semipolar (1122) Bulk GaN Substrate,” 2007, Electron Letter, vol. 43, No. 15, pp. 825-826.
Zhong et al., “High Power and High Efficiency Blue Light Emitting Diode on Freestanding Semipolar (1122) Bulk GaN Substrate,” 2007, Applied Physics Letter, vol. 90, No. 23, pp. 233504-233504-3.
Lide et al., ‘Thermal Conductivity of Ceramics and Other Insulating Materials,’ CRC Handbook of Chemistry and Physics, 91st Edition, 2010-2011, pp. 12-203 and 12-204.
http://www.matbase.com/material/non-ferrous-metals/other/molybdenum/properties, Data Table for: Non-Ferrous Metals: Other Metals: Molybdenum.
Pattison et al., ‘Gallium Nitride Based Microcavity Light Emitting Diodes With 2λ Effective Cavity Thickness’, Applied Physics Letters, vol. 90, Issue 3, 031111 (2007) 3pg.
USPTO Office Action for U.S. Appl. No. 12/133,364 dated Nov. 26, 2010.
USPTO Office Action for U.S. Appl. No. 12/133,364 dated Jun. 1, 2011.
USPTO Notice of Allowance for U.S. Appl. No. 12/133,364 dated Oct. 11, 2011.
USPTO Office Action for U.S. Appl. No. 12/133,365 dated Jun. 9, 2011.
USPTO Office Action for U.S. Appl. No. 12/133,365 dated Oct. 18, 2011.
USPTO Office Action for U.S. Appl. No. 12/334,418 dated Apr. 5, 2011.
USPTO Office Action for U.S. Appl. No. 12/334,418 dated Oct. 19, 2011.
USPTO Office Action for U.S. Appl. No. 12/478,736 dated Sep. 27, 2011.
USPTO Office Action for U.S. Appl. No. 12/478,736 dated Feb. 7, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/478,736 dated Apr. 23, 2012.
USPTO Office Action for U.S. Appl. No. 12/484,095 dated Nov. 10, 2010.
USPTO Office Action for U.S. Appl. No. 12/484,095 dated Jul. 8, 2011.
USPTO Office Action for U.S. Appl. No. 12/497,969 dated Feb. 2, 2012.
USPTO Office Action for U.S. Appl. No. 12/534,838 dated May 3, 2011.
USPTO Office Action for U.S. Appl. No. 12/534,838 dated Jan. 13, 2012.
USPTO Office Action for U.S. Appl. No. 12/534,838 dated Mar. 20, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/534,838 dated Jun. 8, 2012.
USPTO Office Action for U.S. Appl. No. 12/534,844 dated Sep. 16, 2010.
USPTO Office Action for U.S. Appl. No. 12/534,844 dated Feb. 2, 2011.
USPTO Office Action for U.S. Appl. No. 12/534,857 dated Sep. 1, 2010.
USPTO Notice of Allowance for U.S. Appl. No. 12/534,857 dated May 27, 2011.
USPTO Office Action for U.S. Appl. No. 12/546,458 dated Jul. 20, 2011.
USPTO Notice of Allowance for U.S. Appl. No. 12/546,458 dated Nov. 28, 2011.
USPTO Office Action for U.S. Appl. No. 12/556,558 dated Sep. 16, 2010.
USPTO Notice of Allowance for U.S. Appl. No. 12/556,558 dated Mar. 22, 2011.
USPTO Office Action for U.S. Appl. No. 12/556,562 dated Sep. 15, 2010.
USPTO Office Action for U.S. Appl. No. 12/556,562 dated Mar. 21, 2011.
USPTO Notice of Allowance for U.S. Appl. No. 12/556,562 dated Jul. 27, 2011.
USPTO Office Action for U.S. Appl. No. 12/569,337 dated May 9, 2012.
USPTO Office Action for U.S. Appl. No. 12/569,841 dated Dec. 23, 2011.
USPTO Office Action for U.S. Appl. No. 12/634,665 dated Apr. 25, 2012.
USPTO Office Action for U.S. Appl. No. 12/724,983 dated Mar. 5, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/754,886 dated May 17, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/754,886 dated Jun. 5, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/754,886 dated Jun. 20, 2012.
USPTO Office Action for U.S. Appl. No. 12/785,404 dated Mar. 6, 2012.
Copel et al., ‘Surfactants in Epitaxial Growth’, Physical Review Letters, Aug. 7, 1989, vol. 63, No. 6, p. 632-635.
Lu et al., ‘Structure of the CI-passivated GaAs(111) surface’, Physical Review B, Nov. 15, 1998, vol. 58, No. 20, pp. 13820-13823.
Massies et al., ‘Surfactant mediated epitaxial growth of InxGal-xAs on GaAs (001)’, Applied Physics Letters, vol. 61, No. 1, Jul. 6, 1992, pp. 99-101.
Sumiya et al., ‘High-pressure synthesis of high-purity diamond crystal’, Diamond and Related Materials, 1996, vol. 5, pp. 1359-1365.
Communication from the Chinese Patent Office re 200980134876.2 dated Jul. 3, 2013.
Communication from the Polish Patent Office re P394857 dated Aug. 14, 2013.
USPTO Office Action for U.S. Appl. No. 12/133,365 dated Aug. 21, 2013, 29 pages.
USPTO Office Action for U.S. Appl. No. 12/334,418 dated Sep. 17, 2013, 27 pages.
USPTO Office Action for U.S. Appl. No. 12/497,969 dated Sep. 6, 2013, 21 pages.
USPTO Office Action for U.S. Appl. No. 12/636,683 dated Aug. 16, 2013, 16 pages.
USPTO Office Action for U.S. Appl. No. 12/697,171 dated Jun. 20, 2013, 17 pages.
USPTO Office Action for U.S. Appl. No. 12/697,171 dated Aug. 20, 2013, 17 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. 12/497,969 dated Jul. 5, 2012.
USPTO Office Action for U.S. Appl. No. 12/534,843 dated Sep. 10, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/534,849 dated Jul. 31, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/785,404 dated Jul. 16, 2012.
USPTO Office Action for U.S. Appl. No. 13/179,346 dated Aug. 17, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 13/425,304 dated Aug. 22, 2012.
Choi et al., ‘2.51 microcavity InGaN light-emitting diodes fabricated by a selective dry-etch thinning process’, Applied Physics Letters, 2007, 91(6), 061120.
Weisbuch et al., ‘Recent results and latest views on microcavity LEDs’, Light-Emitting Diodes: Research, Manufacturing, and Applications VIII, ed. By S.A. Stockman et al., Proc. SPIE, vol. 5366, p. 1-19 (2004).
USPTO Notice of Allowance for U.S. Appl. No. 12/478,736 dated Oct. 9, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/569,337 dated Nov. 15, 2012.
USPTO Office Action for U.S. Appl. No. 12/569,844 dated Oct. 12, 2012.
USPTO Office Action for U.S. Appl. No. 12/634,665 dated Oct. 1, 2012.
USPTO Office Action for U.S. Appl. No. 12/891,668 dated Sep. 25, 2012.
USPTO Office Action for U.S. Appl. No. 13/025,833 dated Jul. 12, 2012.
USPTO Office Action for U.S. Appl. No. 13/041,199 dated Nov. 30, 2012.
USPTO Office Action for U.S. Appl. No. 13/175,739 dated Dec. 7, 2012.
USPTO Office Action for U.S. Appl. No. 13/179,346 dated Dec. 13, 2012.
USPTO Office Action for U.S. Appl. No. 13/226,249 dated Oct. 10, 2012.
USPTO Notice of Allowance for U.S. Appl. No. 12/534,843 dated Jan. 24, 2013.
Communication from the Polish Patent Office re P394857 dated Jan. 22, 2013, 2 pages.
USPTO Notice of Allowance for U.S. Appl. No. 12/634,665 dated Feb. 15, 2013.
USPTO Office Action for U.S. Appl. No. 13/041,199 dated Mar. 12, 2013.
USPTO Notice of Allowance for U.S. Appl. No. 13/226,249 dated Feb. 21, 2013.
Related Publications (1)
Number Date Country
20120091465 A1 Apr 2012 US
Provisional Applications (1)
Number Date Country
61392565 Oct 2010 US