分子束外延合成 In2Se3 薄膜

Cooper A. Voigt, Matthew Reingold, Alex Dube, Lawrence S. Early, Brent K. Wagner, Eric M. Vogel
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摘要

介绍了基底选择、基底温度、硒/铟通量比和沉积后冷却速度对分子束外延合成的硒化铟薄膜的相组成、表面形貌和化学计量学的影响。In2Se3 薄膜是在蓝宝石、Si(111) 和高取向热解石墨 (HOPG) 基质上合成的。分别通过拉曼光谱、X 射线光电子能谱和原子力显微镜对薄膜的相组成、化学计量学和表面形貌进行了表征。在所有基底上,较高的基底温度和较高的硒/铟比促进了β-In2Se3的形成,而不是γ和/或κ-In2Se3。在所有基底上,随着基底温度的升高,In2Se3 薄片的横向尺寸也随之增大,在 973 K 时,在 HOPG 上观察到的 β-In2Se3 薄片的横向尺寸最大。以 1200、120 和 12 K/h 的速度冷却 HOPG 上的 β-In2Se3 薄膜,没有观察到 β 到 α-In2Se3 相转变的迹象。在 In2Se3 粉末随温度变化的 XRD 中观察到了一些从 β 到 α-In2Se3 相转变的证据,这表明除了冷却速度之外,还有另一个参数将 In2Se3 薄膜锁定为 β 相。
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Molecular beam epitaxy synthesis of In2Se3 films
The effects of substrate choice, substrate temperature, Se/In flux ratio, and cooling rate after deposition on the phase composition, surface morphology, and stoichiometry of indium selenide films synthesized via molecular beam epitaxy are presented. In2Se3 films were synthesized on sapphire, Si(111) and highly oriented, pyrolytic graphite (HOPG) substrates. The phase composition, stoichiometry, and surface morphology of the films were characterized via Raman spectroscopy, x-ray photoelectron spectroscopy, and atomic force microscopy, respectively. Higher substrate temperature combined with higher Se/In ratio promoted formation of β-In2Se3 over γ and/or κ-In2Se3 on all substrates. Higher Se/In ratio also independently promoted β-In2Se3 over γ and/or κ-In2Se3 on all substrates at 673 K. The lateral dimensions of In2Se3 flakes increased as the substrate temperature increased on all substrates, and the largest lateral dimensions were observed for β-In2Se3 flakes on HOPG at 973 K. No evidence of α-In2Se3 was observed in the Raman spectra of any of the films at any of the synthesis conditions in this study. β-In2Se3 films on HOPG were cooled at 1200, 120, and 12 K/h and no evidence of a β to α-In2Se3 phase transition was observed. Some evidence of β to α-In2Se3 phase transition was observed in temperature-dependent XRD of In2Se3 powders, suggesting that another parameter besides cooling rate is locking the In2Se3 films into the β-phase.
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