US2023407521A1PendingUtilityA1

Group iii nitride single crystal substrate

Assignee: TOKUYAMA CORPPriority: Sep 22, 2017Filed: Aug 15, 2023Published: Dec 21, 2023
Est. expirySep 22, 2037(~11.1 yrs left)· nominal 20-yr term from priority
H10P 14/3416H10P 14/2908H10P 14/36H10P 14/24H10P 14/20H10P 14/2925H10H 20/0137C30B 29/403C23C 16/0209C23C 16/34C30B 25/186C30B 25/20H01L 21/02389H01L 21/0254H01L 21/0262H01L 21/02634H01L 21/02658H01L 33/0075C23C 14/0617C30B 23/025C23C 16/303C23C 14/02C23C 14/26C23C 14/243C30B 29/38
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Claims

Abstract

A group III nitride single crystal substrate including a main surface, the main surface including: a center; a periphery; an outer region whose distance from the center is greater than 30% of a first distance, the first distance being a distance from the center to the periphery; and an inner region whose distance from the center is no more than 30% of the first distance, wherein a ratio (v A −v B )/v B is within the range of ±0.1%, wherein v A is a minimum value of peak wave numbers of micro-Raman spectra in the inner region; and v B is an average value of peak wave numbers of micro-Raman spectra in the outer region.

Claims

exact text as granted — not AI-modified
1 . A method for producing an aluminum nitride single crystal substrate, the method comprising, in the sequence set forth:
 (a) thermally treating a base substrate at a constant temperature of 1000 to 2300° C. for at least 60 seconds, wherein the base substrate is an aluminum nitride single crystal substrate comprising a main surface; and   (b) growing an aluminum nitride single crystal layer over the main surface by means of vapor phase epitaxy, wherein the main surface has a surface roughness of no more than 0.5 nm in terms of arithmetical mean height Sa.   
     
     
         2 . The method according to  claim 1 ,
 wherein the thermal treatment in the (a) is carried out while supplying a halogen gas, a hydrogen halide gas, and/or ammonia gas.   
     
     
         3 . The method according to  claim 1 ,
 wherein the thermal treatment in the (a) is carried out at the constant temperature of 1000 to 1700° C.   
     
     
         4 . The method according to  claim 1 ,
 wherein the vapor phase epitaxy in the (b) is hydride vapor phase epitaxy.   
     
     
         5 . The method according to  claim 1 ,
 wherein the thermally treating in (a) is carried out at a constant temperature within the range of ±100° C. from a temperature of the substrate in (b).

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