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In situ infrared spectroscopy study of the surface reactions during the atomic layer deposition of TiO2 on GaAs (100) surfaces

机译:GaAs(100)表面TiO2原子层沉积过程中表面反应的原位红外光谱研究

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The surface reactions during the atomic layer deposition (ALD) of TiO2 on chemical oxide and hydrogen fluoride etched GaAs (100) surfaces at 100 and 200 degrees C have been studied by in situ attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Tetrakis (dimethylamino) titanium (TDMAT) and H2O were used as precursors. The adsorption of TDMAT on both GaAs surfaces at 200 degrees C was self-limiting, while significant contribution from physisorption was confirmed at 100 degrees C. In addition to the basic ligand substitution mechanism, the presence of parallel/competing reaction pathways was confirmed through the detection of Ti metallacycles and methylmethyleneimine [CH3N=CH2] (MMI). Isotope exchange experiments using D2O and H-2 O-18 were used to confirm the presence of MMI. This product was produced at each H2O exposure step and partially removed during the subsequent TDMAT exposure leading to its accumulation in the growing film. (C) 2017 Elsevier B.V. All rights reserved.
机译:通过原位衰减全反射傅里叶变换红外(ATR-FTIR)光谱研究了TiO2在化学氧化物和氟化氢蚀刻的GaAs(100)表面在TiO2的原子层沉积(ALD)期间的表面反应。四(二甲基氨基)钛(TDMAT)和H2O被用作前体。 TDMAT在200摄氏度时在两个GaAs表面上的吸附是自限性的,而在100摄氏度时证实了物理吸附的显着贡献。除了基本的配体取代机理外,通过钛金属环和甲基亚甲基亚胺[CH3N = CH2](MMI)的检测。使用D2O和H-2 O-18进行的同位素交换实验用于确认MMI的存在。该产品在每个H2O暴露步骤生产,并在随后的TDMAT暴露过程中部分除去,导致其在生长膜中积累。 (C)2017 Elsevier B.V.保留所有权利。

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