Transparent group III metal nitride and method of manufacture

Abstract

Large-area, low-cost single crystal transparent gallium-containing nitride crystals useful as substrates for fabricating GaN devices for electronic and/or optoelectronic applications are disclosed. The gallium-containing nitride crystals are formed by controlling impurity concentrations during ammonothermal growth and processing to control the relative concentrations of point defect species.

Claims

1. A gallium-containing nitride crystal comprising: a top surface having a crystallographic orientation within about 5 degrees of a plane selected from a (0001)+c-plane and a (000-1)c-plane; a substantially wurtzite structure; n-type electronic properties; an impurity concentration greater than about 210.sup.17 cm.sup.3 of hydrogen; an impurity concentration less than about 110.sup.17 cm.sup.3 of oxygen; an H/O ratio of at least 10; an impurity concentration greater than about 210.sup.14 cm.sup.3 of at least one of Li, Na, K, Rb, Cs, Ca, F, and Cl; an optical absorption coefficient less than about 5 cm.sup.1 at a wavelength of 400 nanometers; an optical absorption coefficient less than about 4 cm.sup.1 at a wavelength of 410 nanometers; an optical absorption coefficient less than about 3 cm.sup.1 at a wavelength of 415 nanometers; and an optical absorption coefficient less than about 2 cm.sup.1 at a wavelength of 450 nanometers; wherein the gallium-containing nitride crystal is characterized by, an absorbance per unit thickness of at least 0.01 cm.sup.1 at wavenumbers of 3218 cm.sup.1, 3202 cm.sup.1, and 3188 cm.sup.1; and no infrared absorption peaks at wavenumbers between about 3175 cm.sup.1 and about 3000 cm.sup.1 having an absorbance per unit thickness greater than 10% of the absorbance per unit thickness at 3218 cm.sup.1.

2. The gallium-containing nitride crystal of claim 1, characterized by a carrier concentration n between about 10.sup.16 cm.sup.3 and 10.sup.20 cm.sup.3 and a carrier mobility , in units of centimeters squared per volt-second, such that the logarithm to the base 10 of is greater than 0.018557[log.sub.10(n)].sup.3+1.0671[log.sub.10(n)].sup.220.599[log.sub.10(n)]+135.49.

3. The gallium-containing nitride crystal of claim 1, further comprising an impurity concentration of at least one of silicon and germanium between about 110.sup.17 cm.sup.3 and about 310.sup.18 cm.sup.3.

4. The gallium-containing nitride crystal of claim 1, wherein the carrier concentration is between about 310.sup.17 cm.sup.3 and about 310.sup.18 cm.sup.3.

5. The gallium-containing nitride crystal of claim 1, wherein the top surface has a diameter greater than about 10 millimeters and the crystal has a thickness greater than about 100 micrometers.

6. The gallium-containing nitride crystal of claim 1, comprising an impurity concentration of at least one of F and Cl between about 210.sup.14 cm.sup.3 and about 510.sup.17 cm.sup.3.

7. A device comprising the gallium-containing nitride crystal of claim 1.

8. A gallium-containing nitride crystal comprising: a top surface having a crystallographic orientation within about 5 degrees of a plane selected from a (0001)+c-plane and a (000-1)c-plane; a substantially wurtzite structure; n-type electronic properties; an impurity concentration greater than about 510.sup.17 cm.sup.3 of hydrogen; an impurity concentration between about 210.sup.17 cm.sup.3 and about 410.sup.18 cm.sup.3 of oxygen; an H/O ratio of at least 0.3; an impurity concentration greater than about 110.sup.16 cm.sup.3 of at least one of Li, Na, K, Rb, Cs, Ca, F, and Cl; an optical absorption coefficient less than about 8 cm.sup.1 at a wavelength of 400 nanometers; an optical absorption coefficient less than about 6 cm.sup.1 at a wavelength of 410 nanometers; an optical absorption coefficient less than about 5.5 cm.sup.1 at a wavelength of 415 nanometers; an optical absorption coefficient less than about 4 cm.sup.1 at a wavelength of 450 nanometers; an absorbance per unit thickness of at least 0.01 cm.sup.1 at wavenumbers of approximately 3175 cm.sup.1, 3164 cm.sup.1, and 3150 cm.sup.1; no infrared absorption peaks at wavenumbers between about 3200 cm.sup.1 and about 3400 cm.sup.1 or between about 3075 cm.sup.1 and about 3125 cm.sup.1 having an absorbance per unit thickness greater than 10% of the absorbance per unit thickness at 3175 cm.sup.1.

9. The gallium-containing nitride crystal of claim 8, characterized by a carrier concentration n between about 10.sup.16 cm.sup.3 and 10.sup.20 cm.sup.3 and a carrier mobility , in units of centimeters squared per volt-second, such that the logarithm to the base 10 of is greater than 0.018557[log.sub.10(n)].sup.3+1.0671[log.sub.10(n)].sup.220.599[log.sub.10(n)]+135.49.

10. The gallium-containing nitride crystal of claim 8, further comprising an impurity concentration of at least one of silicon and germanium between about 110.sup.17 cm.sup.3 and about 310.sup.18 cm.sup.3.

11. The gallium-containing nitride crystal of claim 8, wherein the carrier concentration is between about 310.sup.17 cm.sup.3 and about 310.sup.18 cm.sup.3.

12. The gallium-containing nitride crystal of claim 8, wherein the top surface has a diameter greater than about 10 millimeters and the crystal has a thickness greater than about 100 micrometers.

13. The gallium-containing nitride crystal of claim 8, characterized by, an optical absorption coefficient less than about 4 cm.sup.1 at a wavelength of 400 nanometers; an optical absorption coefficient less than about 3 cm.sup.1 at a wavelength of 410 nanometers; an optical absorption coefficient less than about 2.5 cm.sup.1 at a wavelength of 415 nanometers; and an optical absorption coefficient less than about 1.5 cm.sup.1 at a wavelength of 450 nanometers.

14. The gallium-containing nitride crystal of claim 8, characterized by, an optical absorption coefficient less than about 3 cm.sup.1 at a wavelength of 400 nanometers; an optical absorption coefficient less than about 2.2 cm.sup.1 at a wavelength of 410 nanometers; an optical absorption coefficient less than about 2.0 cm.sup.1 at a wavelength of 415 nanometers; and an optical absorption coefficient less than about 1.0 cm.sup.1 at a wavelength of 450 nanometers.

15. A device comprising the gallium-containing nitride crystal of claim 8.

16. A gallium-containing nitride crystal comprising: a top surface having a crystallographic orientation within about 5 degrees of a {1 0-1 0} m-plane; a substantially wurtzite structure; n-type electronic properties; an impurity concentration greater than about 310.sup.18 cm.sup.3 of hydrogen; an impurity concentration between about 510.sup.17 cm.sup.3 and about 310.sup.19 cm.sup.3 of oxygen; an H/O ratio of at least 1.1; an impurity concentration greater than about 110.sup.16 cm.sup.3 of at least one of Li, Na, K, Rb, Cs, Ca, F, and Cl; an optical absorption coefficient less than about 8 cm.sup.1 at a wavelength of 400 nanometers; an optical absorption coefficient less than about 6 cm.sup.1 at a wavelength of 410 nanometers; an optical absorption coefficient less than about 5.5 cm.sup.1 at a wavelength of 415 nanometers; an optical absorption coefficient less than about 4 cm.sup.1 at a wavelength of 450 nanometers; an absorbance per unit thickness of at least 0.01 cm.sup.1 at 3188 cm.sup.1, 3175 cm.sup.1, 3164 cm.sup.1, and 3150 cm.sup.1; and no infrared absorption peaks at wavenumbers between about 3125 cm.sup.1 and about 3000 cm.sup.1, having an absorbance per unit thickness greater than 10% of the absorbance per unit thickness at 3188 cm.sup.1.

17. The gallium-containing nitride crystal of claim 16, characterized by a carrier concentration n between about 10.sup.16 cm.sup.3 and 10.sup.20 cm.sup.3 and a carrier mobility , in units of centimeters squared per volt-second, such that the logarithm to the base 10 of is greater than 0.018557[log.sub.10(n)].sup.3+1.0671[log.sub.10(n)].sup.220.599[log.sub.10(n)]+135.49.

18. The gallium-containing nitride crystal of claim 16, wherein the absorbance per unit thickness at 3232 cm.sup.1 is at least 0.01 cm.sup.1.

19. The gallium-containing nitride crystal of claim 16, further comprising an impurity concentration of at least one of silicon and germanium between about 110.sup.17 cm.sup.3 and about 310.sup.18 cm.sup.3.

20. The gallium-containing nitride crystal of claim 16, wherein the carrier concentration is between about 310.sup.17 cm.sup.3 and about 310.sup.18 cm.sup.3.

21. The gallium-containing nitride crystal of claim 16, wherein the top surface has a diameter greater than about 10 millimeters and the crystal has a thickness greater than about 100 micrometers.

22. A device comprising the gallium-containing nitride crystal of claim 16.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) 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.

(2) FIG. 1 shows infrared spectra of a gallium-containing nitride according to the prior art.

(3) FIG. 2 shown optical absorption coefficients of a gallium-containing nitride crystal measured as a function of wavelength according to certain embodiments of the invention.

(4) FIG. 3 shows infrared spectra of a gallium-containing nitride crystal according to certain embodiments of the invention.

(5) FIG. 4 shows optical absorption coefficients of the four slices from the first free-standing, c-plane ammonothermal gallium-containing nitride crystal, as a function of wavelength, according to certain embodiments of the invention.

(6) FIG. 5 shows measured results of infrared spectra of gallium-containing nitride crystals according to certain embodiments of the invention.

(7) FIG. 6 shows measured results of infrared spectra of a gallium-containing nitride crystal according to certain embodiments of the invention.

(8) FIG. 7 depicts absorption coefficients of gallium-containing nitride crystals, measured as a function of wavelength, according to certain embodiments of the invention.

(9) FIG. 8 shows optical absorption coefficients of two gallium-containing nitride crystals measured as a function of wavelength according to certain embodiments of the invention.

(10) FIG. 9 shows measured results of infrared spectra of two gallium-containing nitride crystals according to certain embodiments of the invention.

(11) FIG. 10 shows crystal shapes and semiconductor devices fabricated on gallium-containing nitride crystals provided by the present disclosure according to certain embodiments.

DETAILED DESCRIPTION

(12) Approximating language, as used herein throughout the specification and claims may be applied to modify any quantitative representation that could permissibly vary without resulting in a change in the basic function to which it may be related. Accordingly, a value modified by a term such as about is not limited to the precise value specified. In at least one instance, the variance indicated by the term about may be determined with reference to the precision of the measuring instrumentation. Similarly, free may be combined with a term; and may include an insubstantial number, or a trace amount, while still being considered free of the modified term unless explicitly stated otherwise.

(13) The metal of a metal nitride may include a group III metal. Suitable metals may include aluminum, gallium, and indium. The one or more refers to combinations of metals in the metal nitride, and may include compositions such as aluminum gallium nitride (AlGaN) and the like. As used herein, the term gallium nitride will be used as an illustrative example of a metal nitride, but it is understood that other group III metal nitrides are also possible.

(14) A metal nitride composition may contain impurities. As used herein, the term impurity refers to a chemical species that is distinct from the group III metal nitride that constitutes the majority composition of the single-crystal or polycrystalline metal nitride. Several classes of impurities may be distinguished with respect to chemistry, atomic structure, intent, and effect. Impurities will generally comprise elements distinct from nitrogen, aluminum, gallium, and indium, including oxygen, carbon, halogens, hydrogen, alkali metals, alkaline earth metals, transition metals, and main block elements. The impurity may be present in a number of forms with different atomic structure. In some cases, the impurity is present as an isolated atom or ion within the crystalline lattice of the group III metal nitride, for example, as a substitutional or interstitial impurity. In other cases, the impurity is present in a distinct phase, for example, as an inclusion within an individual group III metal nitride grain or within a grain boundary of the group III metal nitride. The impurity may be deliberately added to enhance the properties of the group III metal nitride in some way, or may be unintentional. Finally, the impurity may or may not have a significant effect on the electrical, crystallographic, chemical, or mechanical properties of the group III metal nitride.

(15) As used herein, and as is commonly used in the art, the term dopant refers to an impurity that is atomically dispersed within the group III metal nitride, for example, as a substitutional impurity, and which is typically added intentionally. With regard to dopants and dopant precursors (collectively dopants unless otherwise indicated), the electrical properties of the group III metal nitride composition may be controlled by adding one or more of such dopants to the above composition during processing. The dopant may also provide magnetic and/or luminescent properties to the group III metal nitride composition. Suitable dopants may include one or more of s or p block elements, transition metal elements, and rare earth elements. Suitable s and p block elements include, for example, silicon, germanium, magnesium, and tin. Other suitable dopants may include transition group elements. Suitable transition group elements include, for example, zinc, iron, or cobalt. Suitable dopants may produce an n-type material, a p-type material, or a semi-insulating material. In some embodiments, oxygen, whether added intentionally or unintentionally, also acts as a dopant.

(16) Suitable dopant concentration levels in a single-crystal or polycrystalline composition may be greater than about 10.sup.10 atoms per cubic centimeter. In one embodiment, the dopant concentration may be in a range of from about 10.sup.10 atoms per cubic centimeter to about 10.sup.15 atoms per cubic centimeter, from about 10.sup.15 atoms per cubic centimeter to about 10.sup.16 atoms per cubic centimeter, from about 10.sup.16 atoms per cubic centimeter to about 10.sup.17 atoms per cubic centimeter, from about 10.sup.17 atoms per cubic centimeter to about 10.sup.18 atoms per cubic centimeter, from about 10.sup.18 atoms per cubic centimeter to about 10.sup.21 atoms per cubic centimeter, or greater than about 10.sup.21 atoms per cubic centimeter.

(17) As used herein, the term getter refers to an impurity that is intentionally added and has a higher chemical affinity for an undesired impurity, for example, oxygen, than the principal metallic constituent of the composition, for example, gallium. The getter may become incorporated into the polycrystalline group III metal nitride in the form of an inclusion, for example, as a metal nitride, a metal halide, a metal oxide, a metal oxyhalide, or as a metal oxynitride. Examples of suitable getters include the alkaline earth metals, scandium, titanium, vanadium, chromium, yttrium, zirconium, niobium, the rare earth metals, hafnium, tantalum, and tungsten, and their nitrides and halides. In some embodiments, the getter impurity can act as both a getter and a dopant, such as magnesium. In other cases, the getter impurity atom has a larger atomic or covalent diameter than gallium and does not become incorporated as a dopant at sufficient levels to modify the electrical properties of the group III metal nitride significantly, and therefore functions predominantly or exclusively as a getter. The getter may be present in the polycrystalline group III metal nitride at a level greater than 100 ppm, from about 100 ppm to about 200 ppm, from about 200 ppm to about 500 ppm, from about 500 ppm to about 0.1%, from about 0.1% to about 0.2%, from about 0.2% to about 0.5%, from about 0.5% to about 2%, from about 2% to about 10%, or greater than 10%. Parts per million (ppm) and % refer to by weight unless otherwise indicated.

(18) In other cases, impurities are unintended and/or undesirable inclusions in the polycrystalline group III metal nitride, and may result from, for example, processing and handling. Other unintentional impurities may result from contaminants in raw materials. Some unintentional impurities may be more closely associated with select raw materials. In some embodiments, the unintentional impurity includes oxygen present as a substitutional impurity, or dopant, in the polycrystalline group III metal nitride at higher than the desired level. In other embodiments, the unintentional impurity includes oxygen present as a group III oxide inclusion, for example, Ga.sub.2O.sub.3, Al.sub.2O.sub.3, and/or In.sub.2O.sub.3. The unintentional oxygen impurity may originate from residual oxygen in the metal raw material, from moisture or O.sub.2 present as an impurity in the gaseous raw materials used in the synthesis process, from moisture generated from outgassing of the reactor components during the synthesis process, or from an air leak in the reactor. In one embodiment, the oxygen content present as Ga.sub.2O.sub.3 or as a substitutional impurity within gallium nitride may be less than about 300 parts per million (ppm). In another embodiment, the oxygen content present as Ga.sub.2O.sub.3 or as a substitutional impurity within gallium nitride may be in a range of from about 300 parts per million to about 100 parts per million, from about 100 parts per million to about 30 parts per million, from about 20 parts per million to about 10 parts per million, from about 10 parts per million to about 3 parts per million, from about 3 parts per million to about 1 part per million, from about 1 part per million to about 0.3 part per million, from about 0.3 part per million to about 0.1 part per million, or less than about 0.1 part per million.

(19) D'Evelyn et al., in U.S. Pat. No. 7,078,731, taught the synthesis of GaN crystals with an optical absorption coefficient less than 5 cm.sup.1 between wavelengths of 465 nanometers and 700 nanometers. Precise values of the optical absorption coefficient were not reported but the same authors reported photographs of crystals having a pronounced yellowish tint (D'Evelyn et al., Bulk GaN crystal growth by the high pressure ammonothermal method, Journal of Crystal Growth 300, 11 (2007)], implying significant optical absorption at blue-to-violet wavelengths. These authors also reported infrared spectra with a series of absorption features between 3000 and 3250 cm.sup., whose intensities were reported to be insensitive to annealing. The most intense peak, at about 3175 cm.sup.1, had an absorbance, relative to the baseline, of about 0.6. Assuming a crystal thickness of about 400 microns, this corresponds to an absorbance per unit thickness of about 15 cm.sup.1. These infrared spectra are shown in FIG. 1, with newly-added peak designations, and provide a point of comparison to the unexpected findings of the present invention. Eight infrared peaks, with a designation and peak wavenumber as reported in Table 1, were extracted from FIG. 8 in U.S. Pat. No. 7,078,731. Quoting from the U.S. Pat. No. 7,078,731, with the exceptions of the insertions enclosed within brackets, Based on predictions of vibrational frequencies of 3100-3470 cm.sup.1 for V.sub.GaH.sub.1-V.sub.GaH.sub.4 (which may overestimate the actual frequencies by about 200 cm.sup.1) and the observation of infrared absorption features at 3020-3050 cm.sup.1 and at 3140 cm.sup.1 in hydrogen-implanted GaN (Weinstein et al., Appl. Phys. Lett. 72, 1703 (1998)), we believe that the absorption peaks between 3150 and 3200 cm.sup.1 (i.e., peaks a.sub.2 and b.sub.1-b.sub.4 in Table 1) in our samples correspond to V.sub.GaH.sub.3 and V.sub.GaH.sub.4, that the absorption peaks observed between 3000 and 3150 cm.sup.1 (i.e., peaks c.sub.1-c.sub.3) in both our crystal and hydrogen-implanted GaN correspond to V.sub.GaH.sub.1 and V.sub.GaH.sub.2, and that other minor peaks may be associated with the presence of other impurities or defects. Thus, the presence of an infrared absorption feature near 3175 cm.sup.1 in GaN crystals grown by the method described herein indicates passivation of gallium vacancies, and the persistence of the infrared feature upon high temperature annealing indicates that this passivation is quite stable.

(20) TABLE-US-00001 TABLE 1 Designation and peak wavenumber values of peaks in infrared spectra of ammonothermally-grown bulk GaN crystals. Peak Peak Wavenumber (cm.sup.1) Peak Wavenumber (cm.sup.1) Designation U.S. Pat. No. 7,078,731 Present Invention a.sub.1 3218 3218 a.sub.2 3201 3202 b.sub.1 3187 3188 b.sub.2 3174 3175 b.sub.3 3163 3164 b.sub.4 3151 3150 c.sub.1 3115 3115 c.sub.2 3108 3108 c.sub.3 3058 3058 c.sub.4 3046 d.sub.1 3232

(21) The D'Evelyn patent teaches four types of hydrogenated gallium-vacancy defects (V.sub.GaH.sub.1, V.sub.GaH.sub.2, V.sub.GaH.sub.3 and V.sub.GaH.sub.4) but does not have specific teaching about the relationship between the defect concentrations and transparency in visible wavelengths nor does it provide any indication of the relationship between crystallographic growth sector and transparency. Other references suggest that the presence of oxygen, in particular, is deleterious to transparency. Van de Walle taught that the energy levels of bare Ga vacancies and mono- and dehydrogenated Ga vacancies lie within the bandgap and therefore would be expected to give rise to sub-bandgap optical absorption, whereas the energy levels of tri- and tetra-hydrogenated Ga vacancies lay close to or within the valence band and therefore should have less or no impact on optical absorption. Van de Walle, Interactions of hydrogen with native defects in GaN, Phys. Rev. B 56, R10020-R10023 (1997). However, to the best of our knowledge, more complicated Ga vacancy configurations have not been analyzed by high level quantum mechanical calculations.

(22) In the absence of any defects or impurities, gallium nitride is quite transparent between wavelengths of 400 nanometers and 800 nanometers. Optical absorption within this range, therefore, can be attributed to defects, most likely, point defects. We have discovered several surprising features of the defect chemistry in ammonothermal GaN that have implications for the preparation of transparent ammonothermal GaN.

(23) First, we find that the impurity concentrations of oxygen and fluorine, in particular, vary by more than an order of magnitude between different crystallographic growth sectors, with considerably lower concentrations being incorporated into the +c-plane (or Ga face) than in the c-plane (N face) or into m-plane. As a consequence, the H/O ratios are very different.

(24) Second, we find, surprisingly, that ammonothermal GaN grown in the c-plane direction can be more transparent than ammonothermal GaN grown in the +c-plane direction despite having more than 10 higher oxygen concentration.

(25) Third, we find, surprisingly, that the transparency of ammonothermal GaN grown in the +c-plane direction or in the m-direction can be improved markedly by annealing, but that the transparency of ammonothermal GaN grown in the c-plane direction is typically relatively unaffected.

(26) Fourth, we find, surprisingly, that there may be seven (7) or even more types of defects associated with partially-hydrogenated gallium vacancies in ammonothermal GaN that may play a critical role in transparency of ammonothermal GaN. Referring to Table 1, peaks c.sub.3 and c.sub.4 (the latter may be visible only when the former is relatively prominent) vary in intensity differently than the other peaks and seem clearly to be due to a distinct species. Similarly, peaks c.sub.1 and c.sub.2 vary in intensity differently than the other peaks and seem clearly to be due to a different, distinct species. The relative intensities of peaks b.sub.2 and b.sub.3 typically remain constant from sample to sample, and therefore these probably result from a single defect species. However, the relative intensity of peak b.sub.4 to peaks b.sub.2 and b.sub.3 varies between different samples and therefore may be due to a different defect species. Peak b.sub.1 sometimes appears together with peaks b.sub.2-b.sub.4 but sometimes appears without these peaks and therefore likely results from a distinct species. The relative intensities of peaks a.sub.1 and a.sub.2, when present, typically remain constant from sample to sample and therefore result from a single species, but these peaks are absent from some samples where one or more of peaks b.sub.1-b.sub.4 are present and so result from a separate defect. Newly discovered peak d.sub.1 appears to represent still another defect. We have discovered that, at least in some cases, the relative intensities of these peaks may be manipulated in such a way so as to produce highly transparent ammonothermal GaN.

(27) A high-quality n-type conductive, transparent, gallium nitride or metal nitride crystal or wafer may be manufactured cost-effectively by the following method.

(28) One or more high-quality gallium nitride seed crystals or plates may be provided. The seed plates may have a minimum lateral dimension of at least one centimeter. In some embodiments, the seed plates have a maximum lateral dimension of at least two centimeters and a minimum lateral dimension of at least one centimeter. In other embodiments, the seed plates have minimum lateral dimensions of at least three centimeters, at least four centimeters, at least five centimeters, at least six centimeters, at least eight centimeters, or at least ten centimeters. In some embodiments, the seed plates are bulk single crystals of gallium nitride. In some embodiments the seed plates are prepared from crystals that were grown by hydride vapor phase epitaxy. In other embodiments, the seed plates are prepared from crystals that were grown ammonothermally. In still other embodiments, the seed plates are prepared from crystals that were grown from solution in a flux. In some embodiments, the dislocation density at the large- area surfaces of the seed plates is less than about 10.sup.7 cm.sup.2. In some embodiments, the dislocation density at the large-area surfaces of the seed plates is less than about 10.sup.6 cm.sup.2, less than about 10.sup.5 cm.sup.2, less than about 10.sup.4 cm.sup.2, less than about 10.sup.3 cm.sup.2, or less than about 10.sup.2 cm.sup.2. In some embodiments, the full width at half maximum of the lowest-order x-ray diffraction line corresponding to the crystallographic orientation of the large-area face is less than 300 arc seconds, less than 150 arc seconds, less than 100 arc seconds, less than 50 arc seconds, less than 40 arc seconds, less than 30 arc seconds, or less than 20 arc seconds.

(29) In one specific embodiment, the orientation of the large-area surfaces of the seed plates is within about 5 degrees, within about 2 degrees, within about 1 degree, within about 0.5 degree, within about 0.2 degree, or within about 0.1 degree of a {1 0-1 0} m-plane. In another specific embodiment, the orientation of the large-area surfaces of the seed plates is within about 5 degrees, within about 2 degrees, within about 1 degree, within about 0.5 degree, within about 0.2 degree, or within about 0.1 degree of a (0 0 01) c-plane. In another specific embodiment, the orientation of the large-area surfaces of the seed plates is within about 5 degrees, within about 2 degrees, within about 1 degree, within about 0.5 degree, within about 0.2 degree, or within about 0.1 degree of a {1 1-2 0} a-plane. In some embodiments, the seed plate has a semi-polar large-surface orientation, which may be designated by (hkil) Bravais-Miller indices, where i=(h+k), l is nonzero and at least one of h and k are non-zero. In a specific embodiment, the orientation of the large-area surfaces of the seed plates is within about 5 degrees, within about 2 degrees, within about 1 degree, within about 0.5 degree, within about 0.2 degree, or within about 0.1 degree of {1-1 01}, {1-1 02}, {1-1 03}, {2 0-21} or {1 1-22}.

(30) The one or more seed plates may be affixed to a seed rack, as described in U.S. Application Publication No. 2010/0031875, which is incorporated by reference in its entirety. If the front and back faces of the seed plates are crystallographically non-equivalent, as with a c-plane or semi-polar orientation, two seed plates may be placed back to back so that the outward facing surfaces have an equivalent crystallographic orientation.

(31) A polycrystalline group III metal nitride or gallium nitride nutrient material may be provided, as described in U.S. Pat. No. 8,461,071 and U.S. Application Publication No. 2011/0220912, each of which is incorporated by reference in its entirety. The polycrystalline group III metal nitride may have an oxygen content in the group III metal nitride material provided as a group III metal oxide or as a substitutional impurity within a group III metal nitride that is less than about 300 parts per million (ppm), less than about 100 ppm, or less than about 10 ppm. The polycrystalline group III metal nitride may comprise a getter at a level of at least 100 ppm with respect to the group III metal, where the getter is selected from at least alkaline earth metals, scandium, titanium, vanadium, chromium, yttrium, zirconium, niobium, rare earth metals, hafnium, tantalum, and tungsten. In certain embodiments, the polycrystalline group III metal nitride comprises at least one of silicon and germanium at a concentration between about 110.sup.16 cm.sup.3 and about 110.sup.19 cm.sup.3 or between about 110.sup.17 cm.sup.3 and about 310.sup.18 cm.sup.3.

(32) The polycrystalline group III metal nitride may be placed in a basket, which is then placed in an autoclave or a capsule, as described in U.S. Pat. Nos. 6,656,615; 7,125,453; and 7,078,731 and in U.S. Application Publication No. 2009/0301388. Ammonia and a mineralizer, for example, at least one of an alkali metal, amide, nitride, or azide, an alkaline earth metal, amide, nitride, or azide, ammonium fluoride, ammonium chloride, a group III metal fluoride, a group III metal chloride, or a reaction product between a group III metal, ammonia, HF, and HCl are also placed in the autoclave or capsule.

(33) In some embodiments a getter is also placed in the autoclave or capsule. The added getter may be provided in addition to a getter composition that may be present in the polycrystalline group III nitride. The added getter may comprise at least one of alkaline earth metals, Sc, Ti, V, Cr, Y, Zr, Nb, Hf, Ta, W, rare earth metals, and their nitrides, halides, oxynitrides, oxyhalides, amides, imides, and azides. In one specific embodiment, at least a portion of the getter is added in the form of a metal and at least a portion of the mineralizer is added as an azide in such a ratio that the hydrogen generated by reaction of the getter metal with ammonia and the nitrogen generated by decomposition of the azide are present in a ratio of approximately 3:1, as described in U.S. Pat. No. 8,323,405. The added getter may be useful for removing unintentional impurities, for example, oxygen, that are present in the mineralizer or other raw material. In one set of embodiments, the mineralizer comprises an alkali metal and the getter comprises a nitride, imide, or amide of Be, Mg, Ca, Sr, Ba, Sc. Y, a rare earth metal, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, or W. In another set of embodiments, the mineralizer comprises Cl and the getter comprises a nitride, chloride, oxynitride, or oxychloride of Sc, Cr, Zr, Nb, Hf, Ta, or W. In still another set of embodiments, the mineralizer comprises F and the getter comprises a nitride, fluoride, oxynitride, or oxyfluoride of Cr, Zr, Nb, Hf, Ta, or W.

(34) After all the raw materials have been added to the autoclave or capsule, the autoclave or capsule is sealed.

(35) The capsule, if employed, is then placed within a suitable high pressure apparatus. In one embodiment, the high pressure apparatus comprises an autoclave, as described by U.S. Pat. No. 7,335,262. In another embodiment, the high pressure apparatus is an internally heated high pressure apparatus, as described in U.S. Pat. No. 7,125,453, and in U.S. Application Publication No. 2006/0177362 A1 and U.S. Pat. No. 8,097,081. The polycrystalline group III metal nitride and seed crystals are then processed in supercritical ammonia at a temperature greater than about 400 degrees Celsius and a pressure greater than about 50 MegaPascal (MPa), during which at least a portion of the polycrystalline group III metal nitride is etched away and recrystallized onto at least one group III nitride crystal with a wurtzite structure. In some embodiments, the polycrystalline group III metal nitride is processed in supercritical ammonia at a temperature greater than about 500 degrees Celsius, greater than about 550 degrees Celsius, greater than about 600 degrees Celsius, greater than about 650 degrees Celsius, greater than about 700 degrees Celsius, or greater than about 750 degrees Celsius. In some embodiments, the polycrystalline group III metal nitride is processed in supercritical ammonia at a pressure greater than about 100 MPa, greater than about 200 MPa, greater than about 300 MPa, greater than about 400 MPa, greater than about 500 MPa, or greater than about 600 MPa.

(36) Residual getter in the polycrystalline group III metal nitride is released into solution gradually as the polycrystalline group III metal nitride is etched. Once in solution, the getter may react to form a getter metal nitride, amide, or halide. The getter may also be chemically bound to oxygen. The getter may remove residual oxygen in the supercritical ammonia solution, enabling growth of group III nitride single crystals with improved purity and transparency.

(37) By growing for a suitable period of time, the ammonothermally-grown crystalline group III metal nitride may have a thickness of greater than about 1 millimeter and a length, or diameter, greater than about 20 millimeters. In certain embodiments, the length is greater than about 50 millimeters or greater than about 100 millimeters. The crystalline group III nitride may be characterized by crystallographic radius of curvature of greater than 1 meter, greater than 10 meters, greater than 100 meters, greater than 1000 meter, or be greater than can be readily measured (infinite). After growth, the ammonothermally-grown crystalline group III metal nitride may be annealed in an inert, oxidizing, nitriding, or reducing atmosphere, for example, comprising one or more of argon, nitrogen, ammonia, oxygen, or hydrogen, at a pressure between about 1 millibar and 10,000 bar or between about 0.1 bar and about 1.1 bar. The annealing may be performed at a temperature between about 800 degree Celsius and about 1500 degree Celsius or between about 950 degrees Celsius and about 1200 degrees Celsius for a period of time in a range of from about 30 minutes to about 200 hours or from about 5 hours to about 50 hours. After growth, the ammonothermally-grown crystalline group III metal nitride may be sliced, lapped, polished, and chemical-mechanically polished according to methods that are known in the art to form one or more wafers or crystalline substrate members. In a specific embodiment, the root-mean-square surface roughness of the at least one wafer or crystalline substrate member is less than about one nanometer, for example, as measured by atomic force microscopy over an area of at least about 10 micrometers by 10 micrometers.

(38) Referring to FIG. 10, in certain embodiments the ammonothermally-grown crystalline group III metal nitride takes the form of a wafer 102, a platelet crystal 104, a hexagonal boule 106, or a rectangular boule 108. Other shapes are also possible, for example, comprising one or more of as-grown (0001), (000-1), {10-10}, {10-1-1}, {10-1-2}, {10-11}, and {10-12} surfaces. In each case one surface of the ammonothermally-grown crystalline group III metal nitride may be designated as a top surface 110. In certain embodiments the top surface comprises one of at most two largest-area surfaces of a free-standing ammonothermally-grown group III metal nitride crystal. In certain embodiments, top surface 110 has growth features such as hillocks and/or etch features such as pits. In certain embodiments, for example, a wafer 102, the top surface 110 has been prepared for epitaxial regrowth, for example, by metalorganic chemical vapor deposition (MOCVD), molecular beam epitaxy, hydride vapor phase epitaxy (HVPE), ammonothermal growth, or flux growth. In certain embodiments, top surface 110 is prepared by chemical mechanical polishing and final cleaning in a clean-room environment.

(39) The ammonothermally-grown crystalline group III metal nitride may be characterized by a wurzite structure substantially free from any cubic entities and have an optical absorption coefficient of about 2 cm.sup.1 and less at wavelengths between about 385 nanometers and about 750 nanometers. An ammonothermally-grown gallium nitride crystal may comprise a crystalline substrate member having a length greater than about 5 millimeters, have a wurtzite structure and be substantially free of other crystal structures, the other structures being less than about 0.1% in volume in reference to the substantially wurtzite structure, an impurity concentration greater than 10.sup.14 cm.sup.3, greater than 10.sup.15 cm.sup.3, or greater than 10.sup.16 cm.sup.3 of at least one of Li, Na, K, Rb, Cs, Mg, Ca, F, Cl, Br, and I and an optical absorption coefficient of about 2 cm.sup.1 and less at wavelengths between about 405 nanometers and about 750 nanometers. The ammonothermally-grown gallium nitride crystal may be semi-insulating, with a resistivity greater than 10.sup.5 -cm, greater than 10.sup.6 -cm, greater than 10.sup.7 -cm, greater than 10.sup.8 -cm, greater than 10.sup.9 -cm, greater than 10.sup.10 -cm, greater than 10.sup.11 -cm, or greater than 10.sup.12 -cm at room temperature. The ammonothermally-grown gallium nitride crystal may be an n-type semiconductor, with a carrier concentration n between about 10.sup.16 cm.sup.3 and 10.sup.20 cm.sup.3 and a carrier mobility , in units of centimeters squared per volt-second, such that the logarithm to the base 10 of is greater than about 0.018557[log.sub.10(n)].sup.3+1.0671[log.sub.10(n)].sup.220.599[log.sub.10(n)]+135.49. In certain embodiments, the logarithm to the base 10 of is greater than about 0.018557[log.sub.10(n)].sup.3+1.0671[log.sub.10(n)].sup.220.599[log.sub.10(n)]+135.59. In certain embodiments, that the logarithm to the base 10 of is greater than about 0.018557[log.sub.10(n)].sup.3+1.0671[log.sub.10(n)].sup.220.599[log.sub.10(n)]+135.69. The ammonothermally-grown gallium nitride crystal may be a p-type semiconductor, with a carrier concentration n between about 10.sup.16 cm.sup.3 and 10.sup.20 cm.sup.3 and a carrier mobility , in units of centimeters squared per volt-second, such that the logarithm to the base 10 of is greater than about 0.6546 log.sub.10(n)+12.809. The optical absorption coefficient of the ammonothermally-grown crystalline group III metal nitride at wavelengths between about 395 nm and about 460 nm may be less than about 10 cm.sup.1, less than about 5 cm.sup.1, less than about 2 cm.sup.1, less than about 1 cm.sup.1, less than about 0.5 cm.sup.1, less than about 0.2 cm.sup.1, or less than about 0.1 cm.sup.1. The optical absorption coefficient of the ammonothermally-grown crystalline group III metal nitride at wavelengths of approximately 400 nm, 410 nm, 420 nm, and/or 450 nm may be less than about 10 cm.sup.1, less than about 5 cm.sup.1, less than about 2 cm.sup.1, less than about 1 cm.sup.1, less than about 0.5 cm.sup.1, less than about 0.2 cm.sup.1, or less than about 0.1 cm.sup.1.

(40) The transparent ammonothermally-grown crystalline group III metal nitride crystal, or a wafer sliced and polished from the crystal, may be used as a substrate for fabrication into optoelectronic and 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 cascade 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.

(41) Referring again to FIG. 10, a transparent ammonothermally-grown crystalline group III metal nitride crystal may be used as a substrate 120 for growth by MOCVD. An n-type layer 122, comprising n-type Al.sub.xIn.sub.yGa.sub.1-x-yN, where 0x, y1, is deposited overlying top surface 110 of substrate 120, thereby transforming top surface 110 from a free surface to a regrowth interface. Active layer 124, which may comprise an AlInGaN multiple quantum well structure, for example, is then deposited overlying n-type layer 122, and p-type layer 126, comprising p-type Al.sub.uIn.sub.vGa.sub.1-x-yN, where 0u, v1, is deposited overlying active layer 124. An electrical contact 128, which may be reflective, may be deposited overlying p-type layer 126. Other layers are also possible.

EXAMPLES

(42) Embodiments provided by the present disclosure are further illustrated by reference to the following examples, which describe crystals, properties of the crystals, and methods of fabricating the crystals provided by the present disclosure. It will be apparent to those skilled in the art that many modifications, both to materials, and methods, may be practiced without departing from the scope of the disclosure.

(43) In the figures, #1 refers to the first free standing crystal, #2 refers to the second free-standing crystal, #3 refers to the third free-standing crystal, and #4 refers to the fourth free-standing crystal.

Comparative Example 1

(44) A first previously-ammonothermally-grown m-plane substrate, approximately 111 micrometers thick was placed in a silver capsule along with a 13.4%-open-area baffle, polycrystalline GaN nutrient, NH.sub.4F mineralizer, and ammonia, and the capsule was sealed. The ratios of GaN nutrient and NH.sub.4F mineralizer to ammonia were approximately 1.85 and 0.091, respectively by weight. The capsule was placed in an internally-heated high pressure apparatus and heated to temperatures of approximately 655 degrees Celsius for the upper, nutrient zone and approximately 685 degrees Celsius for the lower, crystal growth zone, maintained at these temperatures for approximately 90 hours, and then cooled and removed. The first m-plane crystal grew to a thickness of approximately 685 micrometers.

(45) The front and back surface of the first m-plane ammonothermal crystal were polished and the optical absorption coefficient measured as a function of wavelength. The results are shown in FIG. 2. Although the crystal was transparent it had a strong yellow tint, with an optical absorption coefficient of approximately 18 cm.sup.1 at a wavelength of 400 nm, approximately 16 cm.sup.1 at =410 nm, approximately 14 cm.sup.1 at =415 nm, and approximately 7 cm.sup.1 at =450 nm, with a wavelength derivative d/d of approximately 0.36 cm.sup.1/nm at =410 nm. The infrared spectrum of the m-plane ammonothermal crystal was measured using a commercial Fourier Transform infrared spectrometer. Referring to Table 1, peaks b.sub.1, b.sub.2, b.sub.3, b.sub.4, c.sub.1, c.sub.2, and c.sub.3 were present, similar to those in the prior-art crystal. However, peaks a.sub.1 and a.sub.2, which were quite prominent in the prior-art crystal, were not visible at all in the first m-plane ammonothermal crystal, proving that different species were responsible for peaks a.sub.1 and a.sub.2 than for peaks b.sub.1, b.sub.2, b.sub.3, and b.sub.4, contradicting the peak assignments in the prior-art reference. In addition, a new peak, c.sub.4, was visible in the spectrum of the first m-plane ammonothermal crystal. The surface impurity composition of this crystal was measured by calibrated secondary ion mass spectrometry (SIMS) yielding levels of 4.210.sup.19 cm.sup.3 for hydrogen, 1.610.sup.19 cm.sup.3 for oxygen, and 8.610.sup.18 cm.sup.3 for fluorine.

Example 1

(46) Four (4) c-plane oriented bulk GaN crystal grown by HVPE, approximately 0.3 millimeters thick, were provided for use as substrates for patterning. On the first substrate, using nLOF2020 as a photoresist, a pattern comprising linear arrays of 50-micrometer-wide by 1-centimeter-long slits, with a pitch diameter of 550 micrometers was defined. On the second and third substrates, using nLOF2020 as a photoresist, a pattern comprising linear arrays of 20-micrometer-wide by 1-centimeter-long slits, with a pitch diameter of 1020 micrometers was defined. On the fourth substrate, using nLOF2020 as a photoresist, a pattern comprising linear arrays of 20-micrometer-wide by 1-centimeter-long slits, with a pitch diameter of 520 micrometers was defined. A 100-nanometer-thick layer of TiW was deposited on each substrate as an adhesion layer, followed by a 20-micrometer-thick inert layer comprising Au. A lift-off process was performed and the residual photoresist was removed to obtain two patterned c-plane substrates. The mask pattern on each substrate comprised domains of m-stripes, with linear openings oriented approximately parallel to <10-10>.

(47) A first patterned c-plane substrate, together with a second previously-ammonothermally-grown m-plane substrate, approximately 116 micrometers thick, and a third previously-ammonothermally-grown m-plane substrate, approximately 70 micrometers thick, was placed in a silver capsule along with a 13.4%-open-area baffle, polycrystalline GaN nutrient, NH.sub.4F mineralizer, and ammonia, and the capsule was sealed. The ratios of GaN nutrient and NH.sub.4F mineralizer to ammonia were approximately 2.27 and 0.092, respectively, by weight. The capsule was placed in an internally-heated high pressure apparatus and heated to temperatures of approximately 653 degrees Celsius for the upper, nutrient zone and approximately 690 degrees Celsius for the lower, crystal growth zone, maintained at these temperatures for approximately 140 hours, and then cooled and removed. Ammonothermal GaN grew through the linear openings in the patterned mask on the first c-plane HVPE GaN substrate, grew laterally, and coalesced fully, forming an ammonothermal GaN layer approximately 200 micrometers thick with a smooth top surface. The HVPE substrate was then removed from the first c-plane, patterned ammonothermal GaN layer, forming a first free-standing, c-plane, ammonothermal crystal approximately 167 micrometers thick. The second m-plane crystal grew to a thickness of approximately 717 micrometers and the third m-plane crystal grew to a thickness of approximately 801 micrometers.

(48) The front and back surface of the second m-plane ammonothermal crystal were polished and the optical absorption coefficient measured as a function of wavelength. The results are shown in FIG. 2. Although the crystal was transparent it had a strong yellow tint, with an optical absorption coefficient of approximately 29 cm.sup.1 at a wavelength of 400 nm, approximately 25 cm.sup.1 at =410 nm, approximately 21.5 cm.sup.1 at =415 nm, and approximately 11 cm.sup.1 at =450 nm, with a wavelength derivative d/d of approximately 0.7 cm.sup.1/nm at =410 nm. The infrared spectrum of the second m-plane ammonothermal crystal was measured using a commercial Fourier Transform infrared spectrometer. The results, which were very similar to those obtained with the first m-plane ammonothermal crystal, are shown in FIG. 3. By comparison to Table 1, it is evident that peaks b.sub.1, b.sub.2, b.sub.3, b.sub.4, c.sub.1, c.sub.2, and c.sub.3 were present, similar to those in the prior-art crystal, with an absorbance per unit thickness of approximately 1.4 cm.sup.1. However, peaks a.sub.1 and a.sub.2, which were quite prominent in the prior-art crystal, were not visible at all in the m-plane ammonothermal crystal, proving that different species are responsible for peaks a.sub.1 and a.sub.2 than for peaks b.sub.1, b.sub.2, b.sub.3, and b.sub.4, contradicting the peak assignments in the prior-art reference. In addition, a new peak, c.sub.4, was visible in the spectrum of the second m-plane ammonothermal crystal.

(49) The third m-plane crystal was placed in a furnace, heated to 1100 degrees Celsius in air, held at this temperature for 24 hours, and cooled. The front and back surfaces of the third, annealed m-plane ammonothermal crystal were polished and the optical absorption coefficient measured as a function of wavelength. The results are shown in FIG. 2. This crystal was transparent and almost colorless, with an optical absorption coefficient of approximately 10 cm.sup.1 at a wavelength of 400 nm, approximately 7 cm.sup.1 at =410 nm, approximately 6 cm.sup.1 at =415 nm, and approximately 3 cm.sup.1 at =450 nm, with a wavelength derivative d/d of approximately 0.3 cm.sup.1/nm at =410 nm. The infrared spectrum of the m-plane ammonothermal crystal was measured using a commercial Fourier Transform infrared spectrometer and the results are shown in FIG. 3. Referring to Table 1, peaks b.sub.1, b.sub.2, b.sub.3, b.sub.4, were still present. However, peaks a.sub.1 and a.sub.2, which were not visible at all in the second, unannealed m-plane ammonothermal crystal, were now apparent. In addition, peaks c.sub.1, c.sub.2, c.sub.3, and c.sub.4, which were quite prominent in the second, unannealed m-plane crystal, were no longer visible, and a new peak, d.sub.1, appeared at 3232 cm.sup.1. The ratios of the peak intensities of the b.sub.2, b.sub.3, and b.sub.4 peaks to that of the b.sub.1 peak were between 20% and 90%, or between 30% and 80%. The ratios of the d.sub.1, a.sub.1, and a.sub.2 peaks to that of the b.sub.1 peak are between 5% and 20%, and the c.sub.1, c.sub.2, c.sub.3, and c.sub.4, peaks were not visible, with a peak intensity less than 10% or less than 5% than that of the b.sub.1 peak.

Example 2

(50) The first free-standing, c-plane, ammonothermal crystal from Example 1 was used as a seed crystal for another crystal growth run. The crystal was placed in a silver capsule along with a 13.4%-open-area baffle, polycrystalline GaN nutrient, NH.sub.4F mineralizer, and ammonia, and the capsule was sealed. The ratios of GaN nutrient and NH.sub.4F mineralizer to ammonia were approximately 2.72 and 0.092, respectively, by weight. The capsule was placed in an internally-heated high pressure apparatus and heated to temperatures of approximately 656 degrees Celsius for the upper, nutrient zone and approximately 687 degrees Celsius for the lower, crystal growth zone, maintained at these temperatures for approximately 140 hours, and then cooled and removed. Ammonothermal GaN grew on both the front and back face of the seed crystal, increasing its thickness to approximately 1.1 millimeter. This first free-standing ammonothermal crystal, together with the second patterned c-plane substrate from Example 1, was placed in a silver capsule along with a 13.4%-open-area baffle, polycrystalline GaN nutrient, NH.sub.4F mineralizer, and ammonia, and the capsule was sealed. The ratios of GaN nutrient and NH.sub.4F mineralizer to ammonia were approximately 2.20 and 0.091, respectively, by weight. The capsule was placed in an internally-heated high pressure apparatus and heated to temperatures of approximately 650 degrees Celsius for the upper, nutrient zone and approximately 685 degrees Celsius for the lower, crystal growth zone, maintained at these temperatures for approximately 140 hours, and then cooled and removed. Ammonothermal GaN grew on both the front and back face of the first free-standing ammonothermal crystal, increasing its thickness to approximately 2.5 millimeters. Ammonothermal GaN grew through the linear openings in the patterned mask on the second c-plane HVPE GaN substrate, grew laterally, and coalesced fully, forming an ammonothermal GaN layer approximately 485 micrometers thick with a smooth top surface. The HVPE substrate was then removed from the second c-plane, patterned ammonothermal GaN layer, forming a second free-standing, c-plane, ammonothermal crystal approximately 485 micrometers thick.

(51) The second free-standing, c-plane, ammonothermal crystal from was then used as a seed crystal for another crystal growth run. The crystal was placed in a silver capsule along with a 13.4%-open-area baffle, polycrystalline GaN nutrient, NH.sub.4F mineralizer, and ammonia, and the capsule was sealed. The ratios of GaN nutrient and NH.sub.4F mineralizer to ammonia were approximately 2.47 and 0.092, respectively, by weight. The capsule was placed in an internally-heated high pressure apparatus and heated to temperatures of approximately 649 degrees Celsius for the upper, nutrient zone and approximately 684 degrees Celsius for the lower, crystal growth zone, maintained at these temperatures for approximately 120 hours, and then cooled and removed. Ammonothermal GaN grew on both the front and back face of the second free-standing, c-plane, ammonothermal crystal, increasing its thickness to approximately 1.2 millimeter.

(52) Samples were then prepared from the first and second free-standing, c-plane ammonothermal crystals. The first free-standing, c-plane ammonothermal crystal was wire-sawed three-times, forming four slices, and the second free-standing, c-plane ammonothermal crystal was wire-sawed once, forming two slices. Portions of each of the slices were polished on both the front and back sides. Separated portions of the slices were placed in a furnace, heated to 1100 degrees Celsius in air, held at this temperature for 24 hours, and cooled. The front and back surfaces of the annealed slices were then polished.

(53) The optical absorption coefficients of the unannealed four slices from the first free-standing, c-plane ammonothermal crystal are shown as a function of wavelength in FIG. 4. The two slices nearer the N-face, surprisingly, were significantly more transparent than the two slices nearer the Ga-face, with an optical absorption coefficient of about 4-6 cm.sup.1 at 400 nm (vs. about 7 cm.sup.1), an optical absorption coefficient of about 3.6-4.5 cm.sup.1 at 410 nm (vs. about 6 cm.sup.1), an optical absorption coefficient of about 3.25-3.6 cm.sup.1 at 415 nm (vs. about 5.7 cm.sup.1), and an optical absorption coefficient of about 1.8 cm.sup.1 at 450 nm (vs. about 3 cm.sup.1). The infrared spectra of the unannealed slice closest to the Ga-face of the second free-standing c-plane ammonothermal crystal and the unannealed slice closest to the N-face of the first free-standing c-plane ammonothermal crystal were measured and the results are shown in FIG. 5 and FIG. 6, respectively. The (unannealed) near-Ga-face slice exhibited absorption peaks at a.sub.1 and a.sub.2, by reference to FIG. 1 and Table 1, in addition to peaks at b.sub.1-b.sub.4 and c.sub.1. However, the intensities of peaks b.sub.3, b.sub.4, and c.sub.1 were considerably lower than those of the m-plane crystals. By contrast, surprisingly, the near-N-face slice exhibited absorption peaks b.sub.2, b.sub.3, and b.sub.4, but not a.sub.1, a.sub.2, or b.sub.1. Impurity concentrations in the unannealed near-Ga-face slice measured by SIMS included 3.410.sup.18 cm.sup.3 hydrogen, 4.410.sup.16 cm.sup.3 oxygen, and 2.410.sup.15 cm.sup.3 fluorine. Impurity concentrations in the unannealed near-N-face slice measured by SIMS included 1.210.sup.18 cm.sup.3 hydrogen, 2.310.sup.18 cm.sup.3 oxygen, and 1.810.sup.17 cm.sup.3 fluorine.

(54) The electrical properties of the third slice from the first free-standing, c-plane ammonothermal crystal were measured before and after annealing using the van der Pauw Hall effect technique with a 0.51 Tesla magnet and a current of 15 mA DC. Before annealing, the carrier concentration was measured as 1.610.sup.18 cm.sup.3 and the Hall mobility as 271 cm.sup.2/V-s. After annealing, the carrier concentration was measured as 2.610.sup.18 cm.sup.3 and the Hall mobility as 236 cm.sup.2/V-s. The electrical properties of the annealed slice nearest the Ga-face from the second free-standing, c-plane ammonothermal crystal were measured by the same technique, yielding a carrier concentration of 7.110.sup.16 cm.sup.3 and a Hall mobility of 623 cm.sup.2/V-s. Before annealing, the second free-standing, c-plane ammonothermal crystal had a resistance that was too high to measure with the Hall technique, indicating semi-insulating behavior and a resistivity higher than about 10.sup.8 -cm.

(55) The optical absorption coefficients of the unannealed and annealed slice nearest the Ga-face from the second free-standing, c-plane ammonothermal crystal are shown as a function of wavelength in FIG. 7. Before annealing, this sample exhibited an optical absorption coefficient of approximately 9.5 cm.sup.1 at a wavelength of 400 nm, approximately 7.4 cm.sup.1 at =410 nm, approximately 7.0 cm.sup.1 at =415 nm, and approximately 4 cm.sup.1 at =450 nm, with a wavelength derivative d/d of approximately 0.14 cm.sup.1/nm at =410 nm. After annealing, this sample exhibited an optical absorption coefficient of approximately 3.7 cm.sup.1 at a wavelength of 400 nm, approximately 2.4 cm.sup.1 at =410 nm, approximately 1.9 cm.sup.1 at =415 nm, and approximately 1.2 cm.sup.1 at =450 nm, with a wavelength derivative d/d of approximately 0.04 cm.sup.1/nm at =410 nm. The infrared spectra of the unannealed and annealed slice nearest the Ga-face from the second free-standing, c-plane ammonothermal crystal were measured using a commercial Fourier Transform infrared spectrometer. The results are shown in FIG. 5. In the unannealed samples, peaks b.sub.1, b.sub.2, and a.sub.1 were prominent, peaks a.sub.2, a.sub.3, and c.sub.1 were barely detectible, and peaks a.sub.4, c.sub.2, c.sub.3, and c.sub.4 were absent. After annealing, only peaks a.sub.1, a.sub.2, and b.sub.1 were visible, with no other peaks detectible, surprisingly. The ratios of the peak intensities of the a.sub.2 and b.sub.1 peaks to that of the a.sub.1 peak were between 30% and 80%, or between 50% and 70%. The b.sub.2, b.sub.3, b.sub.4, c.sub.1, c.sub.2, c.sub.3, and c.sub.4, peaks were not visible, with a peak intensity less than 10% or less than 5% than that of the a.sub.1 peak. The absorbance per unit thickness of the most intense peak, a.sub.1, was about 0.3 cm.sup.1 (sample thickness was approximately 300 micrometers). Before annealing, the impurity concentrations measured by SIMS included 410.sup.18 cm.sup.3 hydrogen, 5.710.sup.16 cm.sup.3 oxygen, and 110.sup.16 cm.sup.3 fluorine. After annealing, the impurity concentrations measured by SIMS included 7.810.sup.17 cm.sup.3 hydrogen, 3.810.sup.16 cm.sup.3 oxygen, and 3.610.sup.14 cm.sup.3 fluorine.

Example 3

(56) The third patterned c-plane substrate from Example 1 was placed in a silver capsule along with a 13.4%-open-area baffle, polycrystalline GaN nutrient, NH.sub.4F mineralizer, and ammonia, and the capsule was sealed. The ratios of GaN nutrient and NH.sub.4F mineralizer to ammonia were approximately 2.37 and 0.092, respectively, by weight. The capsule was placed in an internally-heated high pressure apparatus and heated to temperatures of approximately 653 degrees Celsius for the upper, nutrient zone and approximately 687 degrees Celsius for the lower, crystal growth zone, maintained at these temperatures for approximately 114 hours, and then cooled and removed. Ammonothermal GaN grew through the linear openings in the patterned mask on the third c-plane HVPE GaN substrate, grew laterally, and coalesced fully, forming an ammonothermal GaN layer approximately 420 micrometers thick with a smooth top surface. The HVPE substrate was then removed from the third c-plane, patterned ammonothermal GaN layer, forming a third free-standing, c-plane, ammonothermal crystal approximately 200 micrometers thick. The third free-standing, c-plane, ammonothermal crystal was placed in a furnace, heated to 1100 degrees Celsius in air, held at this temperature for 30 hours, and cooled.

(57) The front and back surface of the third free-standing, c-plane, ammonothermal crystal were smoothed by etching in hot phosphoric acid and the optical absorption coefficient measured as a function of wavelength. The results are shown in FIG. 7. The crystal was transparent and virtually colorless, with an optical absorption coefficient aof approximately 2.4 cm.sup.1 at a wavelength of 400 nm, approximately 1.5 cm.sup.1 at =410 nm, approximately 1.2 cm.sup.1 at =415 nm, and approximately 0.67 cm.sup.1 at =450 nm, with a wavelength derivative d/d of approximately 0.06 cm.sup.1/nm at =410 nm.

Example 4

(58) The fourth patterned c-plane substrate from Example 1 was placed in a silver capsule along with a 13.4%-open-area baffle, polycrystalline GaN nutrient, NH.sub.4F mineralizer, and ammonia, and the capsule was sealed. Considerable cares was taken to eliminate sources of impurity contaminations from the polyGaN nutrient, the silver capsule, the mineralizer and the ammonia prior to sealing, including applying the teaching of U.S. patent application Ser. No. 14/033,107, which is incorporated by reference in its entirety. The ratios of GaN nutrient and NH.sub.4F mineralizer to ammonia were approximately 1.60 and 0.090, respectively, by weight. The capsule was placed in an internally-heated high pressure apparatus and heated to temperatures of approximately 656 degrees Celsius for the upper, nutrient zone and approximately 680 degrees Celsius for the lower, crystal growth zone, maintained at these temperatures for approximately 164 hours, and then cooled and removed. Ammonothermal GaN grew through the linear openings in the patterned mask on the fourth c-plane HVPE GaN substrate, grew laterally, and coalesced fully, forming an ammonothermal GaN layer approximately 267 micrometers thick with a smooth top surface. The HVPE substrate was then removed from the fourth c-plane, patterned ammonothermal GaN layer, forming a fourth free-standing, c-plane, ammonothermal crystal approximately 250 micrometers thick.

(59) The fourth free-standing, c-plane, ammonothermal crystal from was then used as a seed crystal for another crystal growth run. The Ga-side of the crystal was metalized with a 100-nanometer-thicker layer of TiW, followed by an 8-micrometer-thick inert layer comprising Au. The crystal was placed in a silver capsule along with a 13.4%-open-area baffle, polycrystalline GaN nutrient, NH.sub.4F mineralizer, and ammonia, and the capsule was sealed. Considerable cares was taken to eliminate sources of impurity contaminations from the polyGaN nutrient, the silver capsule, the mineralizer and the ammonia prior to sealing. The ratios of GaN nutrient and NH.sub.4F mineralizer to ammonia were approximately 2.85 and 0.090, respectively, by weight. The capsule was placed in an internally-heated high pressure apparatus and heated to temperatures of approximately 657 degrees Celsius for the upper, nutrient zone and approximately 680 degrees Celsius for the lower, crystal growth zone, maintained at these temperatures for approximately 281 hours, and then cooled and removed. Ammonothermal GaN grew only on the N-polar side of the fourth free-standing, c-plane, ammonothermal crystal, increasing its thickness to approximately 1.8 millimeters.

(60) The fourth free-standing, c-plane, ammonothermal crystal was sliced to completely remove the seed crystal, leaving behind only the N-polar side grown material from the second re-growth. This material was then was double side lapped and polished to a final thickness of 420 micrometers. The N-face slice from the fourth free-standing, c-plane, ammonothermal crystal was transparent and virtually colorless, with an absorption coefficient of approximately 3.1 cm.sup.1 at =400 nm, approximately 2.1 cm.sup.1 at =410 nm, approximately 1.8 cm.sup.1 at =415 nm, and approximately 1.0 cm.sup.1 at =450 nm, with a wavelength derivative d/d of approximately 0.07 cm.sup.1/nm at =410 nm, as shown in FIG. 8. After annealing at 1100 C. in air for 12 hours, this crystal exhibited very little change in optical absorption behavior, surprisingly. The annealed crystal had an absorption coefficient of approximately 2.9 cm.sup.1 at a wavelength of 400 nm, approximately 2.0 cm.sup.1 at =410 nm, approximately 1.7 cm.sup.1 at =415 nm, and approximately 0.8 cm.sup.1 at =450 nm, with a wavelength derivative d/d of approximately 0.07 cm.sup.1/nm at =410 nm, as shown in FIG. 8.

(61) The electrical properties of the N-face slice from the fourth free-standing, c-plane, ammonothermal crystal were measured after annealing using the van der Pauw Hall effect technique, yielding a carrier concentration of 1.110.sup.18 cm.sup.3 and a Hall mobility of 300 cm.sup.2/V-s.

(62) The infrared spectra of the as-grown and annealed N-sector only material obtained from the N slice from the fourth c-plane ammonothermal crystal were measured using a commercial Fourier Transform infrared spectrometer. The results are shown in FIG. 9. Surprisingly, in both the as-grown and annealed samples only exhibited peaks b.sub.1, b.sub.2, b.sub.3, and b.sub.4, but not a.sub.1 or a.sub.2. Also surprising wass the lack of change in IR absorption spectra between as-grown and annealed crystals. The ratios of the peak intensities of the b.sub.3 and b.sub.4 peaks to that of the b.sub.2 peak were between 10% and 90% or between 15% and 85%. Approximately similar peak intensity ratios were observed with the unannealed slice closest to the N-face of the first free-standing c-plane ammonothermal crystal (FIG. 6), although in this case the b.sub.4 peak had a higher peak amplitude than the b.sub.3 peak whereas the reverse was true with the N-face slice from the fourth free-standing c-plane ammonothermal crystal (FIG. 9). The b.sub.1 and c.sub.3 peaks were visible in the spectrum from the annealed, N-face slice from the fourth free-standing c-plane ammonothermal crystal (FIG. 9), with peak amplitudes between 5% and 25% of that of the b.sub.2 peak, but it is not clear whether or not these peaks were present in the spectrum of the unannealed slice closest to the N-face of the first free-standing c-plane ammonothermal crystal (FIG. 6). The a.sub.1, a.sub.2, c.sub.1, and c.sub.2, peaks were not visible in either N-slice crystal, with a peak intensity less than 10% or less than 5% than that of the b.sub.2 peak. The impurity concentrations of the fourth free-standing, c-plane, ammonothermal crystal measured by SIMS after annealing included 1.610.sup.18 cm.sup.3 hydrogen, 1.910.sup.18 cm.sup.3 oxygen, and 5.310.sup.16 cm.sup.3 fluorine. These values were close to the results obtained from the as-grown N-face slice mentioned in example 2, providing further evidence for at most minor changes in defect concentrations during annealing of N-sector ammonothermal GaN material. Surprisingly, the N slice from the fourth free-standing, c-plane, ammonothermal crystal was significantly more transparent than as-grown Ga slice from the second and third free-standing, c-plane, ammonothermal crystals and almost as transparent as these Ga slices after annealing despite having an oxygen concentration higher by more than a factor of ten. In particular, the optical absorption coefficient was less than about 4 cm.sup.1 or less than about 3 cm.sup.1 at a wavelength of 400 nanometers, the optical absorption coefficient was less than about 3 cm.sup.1 or less than about 2.2 cm.sup.1 at a wavelength of 410 nanometers, the optical absorption coefficient was less than about 2.5 cm.sup.1 or less than about 2.0 cm.sup.1 at a wavelength of 415 nanometers, and the optical absorption coefficient was less than about 1.5 cm.sup.1 or less than about 1.0 cm.sup.1 at a wavelength of 450 nanometers.

(63) 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 present invention, which is defined by the appended claims.