JP4342573B2 - Method for growing compound semiconductor thin films - Google Patents
Method for growing compound semiconductor thin films Download PDFInfo
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- JP4342573B2 JP4342573B2 JP2007144842A JP2007144842A JP4342573B2 JP 4342573 B2 JP4342573 B2 JP 4342573B2 JP 2007144842 A JP2007144842 A JP 2007144842A JP 2007144842 A JP2007144842 A JP 2007144842A JP 4342573 B2 JP4342573 B2 JP 4342573B2
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Description
本発明は、V族材料に窒素を用いたIII-V族化合物半導体のエピタキシャル結晶を有機金属気相成長法(MOCVD)により成長する技術に関するものである。 The present invention relates to a technique for growing an epitaxial crystal of a III-V compound semiconductor using nitrogen as a group V material by metal organic chemical vapor deposition (MOCVD).
V族材料に窒素を用いたIII-V族化合物半導体エピタキシャル結晶をMOCVDにより結晶成長するとき、窒素材料となるアンモニア(NH3)はフォスフィン(PH3)、アルシン(AsH3)に比べ、分解効率が著しく低い。このために窒化物系では一般的に他のIII-V化合物半導体に比べ、高温度成長や高V/III比率成長が必要とされる。高温度成長ではIII族材料やドーパント材料の蒸発が発生し、ガリウム(Ga)より蒸気圧の高いアルミニウム(Al)やインジウム(In)を含んだ材料の成長を困難とする。一方、成長温度を下げるとNH3が分解されないことから高V/III比率成長が必要とされ、過剰なNH3がIII族有機材料やドーパント有機材料と錯体を形成し、結晶成長を妨げることから低温度結晶性は困難とされてきた。 When III-V compound semiconductor epitaxial crystals using nitrogen as the group V material are grown by MOCVD, ammonia (NH 3 ), the nitrogen material, is decomposed more efficiently than phosphine (PH 3 ) and arsine (AsH 3 ). Is extremely low. For this reason, nitride systems generally require higher temperature growth and higher V / III ratio growth than other III-V compound semiconductors. High-temperature growth causes evaporation of group III materials and dopant materials, making it difficult to grow materials containing aluminum (Al) and indium (In), which have higher vapor pressures than gallium (Ga). On the other hand, if the growth temperature is lowered, NH 3 is not decomposed, so a high V / III ratio growth is required, and excess NH 3 forms a complex with a group III organic material or dopant organic material, preventing crystal growth. Low temperature crystallinity has been considered difficult.
MOCVDによるエピタキシャル結晶成長において、一般的な材料であるNH3を用いて高品質な窒化物を成長する場合、1000℃程度の高温成長が必要となる。しかし、1000℃を超える高温成長では高いIn組成のInGaNの成長は困難であり、In組成が10%以上のInGaN薄膜成長は780℃以下の低温成長が必要である。しかし、780℃以下の低温ではNH3が十分に分解せず多量な材料を消費しても高In 組成のInGaN薄膜を得ることは難しかった。 In epitaxial crystal growth by MOCVD, when growing high quality nitride using NH 3 which is a general material, high temperature growth of about 1000 ° C. is required. However, growth of InGaN with a high In composition is difficult at high temperature growth exceeding 1000 ° C., and growth of InGaN thin film with an In composition of 10% or more requires low temperature growth at 780 ° C. or less. However, at a low temperature of 780 ° C. or lower, NH 3 is not sufficiently decomposed and it is difficult to obtain an InGaN thin film having a high In composition even if a large amount of material is consumed.
上記の課題を解決するために、本発明ではNH3にTEAを混合し相互化学反応過程により窒素の分解効率を高め600℃の低温度でGaN及び高In組成のInGaN薄膜のエピタキシャル結晶成長を達成している。 In order to solve the above-mentioned problems, in the present invention, TEA is mixed with NH 3 to increase the decomposition efficiency of nitrogen through a mutual chemical reaction process, and achieve epitaxial crystal growth of GaN and InGaN thin films with a high In composition at a low temperature of 600 ° C. is doing.
本発明によるエピタキシャル結晶成長方法を用いれば、600℃の低温度でGaN及び高In 組成のInGaN薄膜を得ることができる。 By using the epitaxial crystal growth method according to the present invention, GaN and an InGaN thin film having a high In composition can be obtained at a low temperature of 600 ° C.
以下に、実施例について図面を参照して説明する。 Embodiments will be described below with reference to the drawings.
GaN薄膜のエピタキシャル結晶成長にはNH3とTEA,トリエチルガリウム(TEG)を用いる。基板にはサファイアを用い、成長前に基板とGaN薄膜との密着性を高めるために800℃に昇温し、トリメチルアルミニウム(TMAl)を2.9μmol/minにて10分間供給、その後降温して成長温度600℃において表1に示す材料供給量で15分間結晶を成長した。TEGの供給停止により成長を終了し、その後、表面状態を整える目的でNH3とTEAの流量を保った状態で800℃に昇温し、30分間保持した後、降温した。図1に示す得られた薄膜のフォトルミネッセンススペクトルにはGaN特有の375nmに発光が観測され、GaN薄膜の成長が確認された。 NH 3 , TEA, and triethylgallium (TEG) are used for epitaxial crystal growth of GaN thin films. Sapphire is used for the substrate, and the temperature is raised to 800 ° C to increase the adhesion between the substrate and the GaN thin film before growth. Crystals were grown at a temperature of 600 ° C. for 15 minutes with the material supply amounts shown in Table 1. The growth was terminated by stopping the supply of TEG, and then the temperature was raised to 800 ° C. while maintaining the flow rates of NH 3 and TEA for the purpose of adjusting the surface state, and the temperature was lowered after holding for 30 minutes. In the photoluminescence spectrum of the obtained thin film shown in FIG. 1, light emission was observed at 375 nm peculiar to GaN, and the growth of the GaN thin film was confirmed.
InGaN薄膜のエピタキシャル結晶成長にはNH3とTEA,トリエチルガリウム(TEG)、トリエチルインジウム(TMI)を用いる。基板にはサファイア上に成長されたGaNを用い、成長温度600℃において表1に示す材料供給量で10分間結晶を成長した。得られたInGaN薄膜は図2に示す二次イオン質量分析法(SIMS)より、In組成60%、Ga組成40%であることが確認された。 NH 3 and TEA, triethylgallium (TEG), and triethylindium (TMI) are used for epitaxial crystal growth of the InGaN thin film. As the substrate, GaN grown on sapphire was used, and a crystal was grown for 10 minutes at a growth temperature of 600 ° C. with the material supply amount shown in Table 1. The obtained InGaN thin film was confirmed to have an In composition of 60% and a Ga composition of 40% by secondary ion mass spectrometry (SIMS) shown in FIG.
本発明に用いる材料供給量 Material supply amount used in the present invention
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JP2016149493A (en) * | 2015-02-13 | 2016-08-18 | 日本エア・リキード株式会社 | Manufacturing method of gallium nitride thin film and gallium nitride thin film |
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