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首页> 外文期刊>Chemical Engineering Science >The kinetics of the low-pressure chemical vapour deposition of molybdenum on silicon from molybdenum hexafluoride and hydrogen
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The kinetics of the low-pressure chemical vapour deposition of molybdenum on silicon from molybdenum hexafluoride and hydrogen

机译:六氟化钼和氢在硅上低压进行钼化学汽相沉积的动力学

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The kinetics of the low-pressure chemical vapour deposition of molybdenum on silicon from molybdenum hexafuloride and hydrogen are studied at 600 K and 8-315 Pa using a continuous flow perfectly mixed reactor,equipped with a microbalance for in situ rate measurements.A significant contribution of reaction of the hexafluoride with silicon,which diffuses through the growing metal layer,to the overall rate obscures the kinetics of the reduction of molybdenum hexafluoride with hydrogen.A model is developed to obtain the intrinsic rates of the latter process.A ten-step elementary surface network is able to describe these rate date.According to this mechanism molybdenum hexafluoride adsorbs on the growing metal surface,leading to adsorbed fluorine atoms and solid molybdenum.The fluorine adatoms are removed from the surface by reaction with adsorbed hydrogen atoms.Trench fill experiments and their modelling furnish additional arguments for the proposed kinetic scheme.
机译:使用配有微量天平的连续流动完全混合反应器,在600 K和8-315 Pa下研究了六氟硼酸钼和氢在硅上进行钼低压化学气相沉积的动力学,该反应器配备了用于原位速率测量的微量天平。扩散穿过生长的金属层的六氟化物与硅的反应对总速率的影响掩盖了六氟化钼被氢还原的动力学。建立了一个模型来获得后一过程的固有速率。十步元素表面网络能够描述这些速率数据。根据这种机理,六氟化钼吸附在生长的金属表面上,导致吸附的氟原子和固态钼。氟原子通过与吸附的氢原子反应从表面去除。实验及其建模为提出的动力学方案提供了更多的论据。

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