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Group iii nitride crystal, method for producing same and method for producing bulk group iii nitride crystal in supercritical ammonia gas

A technology of nitride crystals and nitrides, applied in chemical instruments and methods, crystal growth, from chemically reactive gases, etc., can solve problems such as limited success

Active Publication Date: 2019-07-09
SIXPOINT MATERIALS +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Thus, while one can attempt to obtain seeds for ammonothermal crystal growth by forming seeds with faster growth methods, one has had limited success in producing seeds via methods that grow crystals faster than the ammonothermal process

Method used

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  • Group iii nitride crystal, method for producing same and method for producing bulk group iii nitride crystal in supercritical ammonia gas
  • Group iii nitride crystal, method for producing same and method for producing bulk group iii nitride crystal in supercritical ammonia gas
  • Group iii nitride crystal, method for producing same and method for producing bulk group iii nitride crystal in supercritical ammonia gas

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0068] Example 1 (growth number 0858)

[0069] GaN crystals are grown by HVPE. A 2" c-plane sapphire substrate with a GaN layer grown by MOCVD was loaded in an HVPE reactor. After slowly changing the substrate temperature to about 1000°C under a constant flow of ammonia and nitrogen, gallium chloride gas was introduced for growth Single crystal GaN. After three hours of growth, the growth temperature was gradually decreased over 13 hours. The temperature was decreased linearly by 100°C over 13 hours, resulting in a temperature decrease rate of 100°C per 13 hours. After a total of 16 hours of growth (3 hours constant temperature and 13 hours gradient temperature), the supply of gallium chloride was discontinued and the boiler was closed. At about 800°C, the supply of ammonia gas was discontinued. The GaN crystals were allowed to cool in the reactor until the temperature reached about 300°C. When the crystal is taken out, the GaN crystal is partially self-separated from the s...

example 2

[0071] Example 2 (grinding / polishing of crystal)

[0072] Both sides of the GaN crystal were ground with a diamond grinder to obtain a GaN wafer with a thickness of 1.1 mm. The FWHM of the X-ray rocking curve for the first side is 1382 arc seconds, while the second side does not exhibit the 002 peak. Then, both sides of the GaN crystal wafer are further ground and polished with a diamond slurry. The total thickness becomes 0.85 mm and the Ra roughness on the nitrogen side is 0.5-0.8 nm and the Ra roughness on the gallium side is 0.8-1.2 nm. The FWHM of the X-ray rocking curve of the first side is improved to 1253 arcseconds. The first side does not have any cracks.

example 3

[0073] Example 3 (Ammoniathermal growth using the obtained GaN crystal)

[0074] The GaN crystal wafer obtained in Example 2 was used as a seed crystal for ammonothermal bulk growth. The high pressure reactor is filled with seeds, sodium metal, flow guides, polycrystalline GaN nutrients and ammonia gas. Then, the high pressure reactor was tightly sealed and heated to about 550°C. After 11 days of growth, bulk GaN crystals with a thickness of about 2.07 mm were obtained. The FWHM improvement of the X-ray rocking curve of the first side is 1048 arc seconds. The crystals also do not have cracks.

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Abstract

In one instance, the invention provides a group III nitride crystal having a first side exposing nitrogen polar c-plane of single crystalline or highly oriented polycrystalline group III nitride and a second side exposing group III polar surface, polycrystalline phase, or amorphous phase of group III nitride. Such structure is useful as a seed crystal for ammonothermal growth of bulk group III nitride crystals. The invention also discloses the method of fabricating such crystal. The invention also discloses the method of fabricating a bulk crystal of group III nitride by ammonothermal method using such crystal.

Description

[0001] Cross References to Related Applications [0002] This application claims the title "Group III Nitride Crystals, Methods of Making the Same, and Methods of Making Crystals in Supercritical Ammonia," filed on December 2, 2014, by Tadao Hashimoto, Inventor, Attorney's Dossier Priority to US Application No. 62 / 086,699, No. SIXPOI-022USPRV1, the contents of which are incorporated herein by reference in their entirety. [0003] This application is also related to the following US patent applications: [0004] Submission on July 8, 2005 by Kenji Fujito, Tadao Hashimoto, and Shuji Nakamura entitled "Method for Growing Group III Nitride Crystals in Supercritical Ammonia Using an Autoclave (METHOD)" FORGROWING GROUP III-NITRIDE CRYSTALS IN SUPERCRITICAL AMMONIA USING ANAUTOCLAVE)", PCT Utility Patent Application No. US2005 / 024239 of Attorney Docket No. 30794.0129-WO-01 (2005-339-1); [0005] Submission by Tadao Hashimoto, Makoto Saito, and Shuji Nakamura on April 6, 2007 entitl...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C30B25/20C30B29/40
CPCC30B29/406C30B7/105C30B25/16
Inventor 桥本忠朗
Owner SIXPOINT MATERIALS