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Epitaxial thin film growth of LiH using a liquid-Li atomic template

机译:使用液态锂原子模板的LiH外延薄膜生长

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We report on the synthesis of lithium hydride (LiH) epitaxial thin films through the hydrogenation of a Li melt, forming abrupt LiH/MgO interface. Experimental and first-principles molecular dynamics studies reveal a comprehensive microscopic picture of the crystallization processes, which sheds light on the fundamental atomistic growth processes that have remained unknown in the vapor-liquid-solid method. We found that the periodic structure that formed, because of the liquid-Li atoms at the film/MgO-substrate interface, serves as an atomic template for the epitaxial growth of LiH crystals. In contrast, films grown on the AlO substrates indicated polycrystalline films with a LiAlO secondary phase. These results and the proposed growth process provide insights into the preparation of other alkaline metal hydride thin films on oxides. Further, our investigations open the way to explore fundamental physics and chemistry of metal hydrides including possible phenomena that emerge at the heterointerfaces of metal hydrides.
机译:我们报告了通过Li熔体的氢化形成突然的LiH / MgO界面来合成氢化锂(LiH)外延薄膜。实验性原理和第一性原理的分子动力学研究揭示了结晶过程的全面微观图像,这揭示了在气液固方法中尚不了解的基本原子生长过程。我们发现,由于在膜/ MgO-衬底界面处的液态Li原子而形成的周期性结构,可作为LiH晶体外延生长的原子模板。相反,在AlO衬底上生长的膜表明具有LiAlO第二相的多晶膜。这些结果和拟议的生长过程为在氧化物上制备其他碱金属氢化物薄膜提供了见识。此外,我们的研究为探索金属氢化物的基本物理和化学方法(包括在金属氢化物的异质界面出现的可能现象)开辟了道路。

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