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Control of crystallographic orientation in diamond synthesis through laser resonant vibrational excitation of precursor molecules

机译:通过前驱物分子的激光共振振动激发控制金刚石合成中的晶体学取向

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Crystallographic orientations determine the optical, electrical, mechanical, and thermal properties of crystals. Control of crystallographic orientations has been studied by changing the growth parameters, including temperature, pressure, proportion of precursors, and surface conditions. However, molecular dynamic mechanisms underlying these controls remain largely unknown. Here we achieved control of crystallographic orientations in diamond growth through a joint experimental and theoretical study of laser resonant vibrational excitation of precursor molecules (ethylene). Resonant vibrational excitation of the ethylene molecules using a wavelength-tunable CO2 laser steers the chemical reactions and promotes proportion of intermediate oxide species, which results in preferential growth of {100}-oriented diamond films and diamond single crystals in open air. Quantum molecular dynamic simulations and calculations of chemisorption energies of radicals detected from our mass-spectroscopy experiment provide an in-depth understanding of molecular reaction mechanisms in the steering of chemical reactions and control of crystallographic orientations. This finding opens up a new avenue for controlled chemical vapor deposition of crystals through resonant vibrational excitations to steer surface chemistry.
机译:晶体学取向决定了晶体的光学,电学,机械和热学性质。通过改变生长参数,包括温度,压力,前驱体比例和表面条件,研究了晶体取向的控制。但是,这些控件背后的分子动力学机制仍然未知。在这里,我们通过前体分子(乙烯)的激光共振振动激发的联合实验和理论研究,实现了金刚石生长中晶体学取向的控制。波长可调的CO 2 激光对乙烯分子的共振振动激发控制了化学反应并促进了中间氧化物种类的比例,从而导致{100}取向金刚石膜和金刚石单晶的优先生长露天的水晶。从我们的质谱实验中检测到的量子分子动力学模拟和自由基的化学吸收能计算,为深入理解化学反应控制和晶体学取向控制中的分子反应机理提供了条件。这一发现为通过共振振动激发来控制表面化学的晶体可控化学气相沉积开辟了一条新途径。

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