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Reaction mechanism of a lanthanum precursor in liquid source metalorganic chemical vapor deposition

机译:镧前驱体在液态源金属有机化学气相沉积中的反应机理

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The reaction mechanism of a lanthanum precursor, tris(dipivaloylmethanato)lanthanum (La(DPM)_3), was investigated in liquid source The metalorganic chemical vapor deposition (MOCVD) of lanthanum oxide films. The behavior of La(DPM)_3 in the gas phase was analyzed under actual CVD conditions by in situ infrared absorption spectroscopy. The infrared band identification was performed using density functional theory calculations. We under calculations. We confirmed that the liquid source delivery using tetrahydrofuran as a solvent supplies a La(DPM)_3 molecule functional molecular structure. The spectroscopic data on the gas-phase reactions were correlated with the characteristics martinis The temperature dependence of the infrared absorption suggests that the thermal decomposition of La(DPM)_3 phase may trigger the film deposition. La(DPM)_3 was only partially decomposed in the gas phase under the actual deposition which indicates that surface reactions rather than gas-phase reactions control dominantly the film deposition.
机译:研究了液态水源中镧前驱体三(二戊甲酰基甲基氨基)镧(La(DPM)_3)的反应机理。氧化镧膜的金属有机化学气相沉积(MOCVD)。 La(DPM)_3在气相中的行为在实际CVD条件下通过原位红外吸收光谱法进行了分析。使用密度泛函理论计算进行红外波段识别。我们正在计算。我们确认使用四氢呋喃作为溶剂的液体源输送提供了La(DPM)_3分子功能性分子结构。气相反应的光谱数据与马提尼酒的特征相关。红外吸收的温度依赖性表明,La(DPM)_3相的热分解可能触发膜沉积。 La(DPM)_3在实际沉积下仅在气相中部分分解,这表明表面反应而非气相反应主要控制了薄膜沉积。

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