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The a-Si:H growth mechanism:temperature study of the SiH_3 surface reactivity and the surface silicon hydride composition during film growth

机译:A-Si:H生长机制:薄膜生长期间SIH_3表面反应性的温度研究和表面硅氢化物组合物

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We report on two experimental studies carried out to reveal insight into the interaction of SiH_3 radicals with the a-Si:H surface as assumed essential in the a-Si:H growth mechanism.The surface reaction probability beta of SiH_3 on the a-Si:H has been investigated by spectroscopic means as a function of the substrate temperature (50-450 degC) using the time-resolved cavity ringdown technique.The silicon hydrides-SiH_x on the a-Si:H surface during deposition have been studied by the combination of in situ attenuated total reflection infrared spectroscopy and argon ion-induced desorption of surface hydrogen.For SiH_3 dominated plasma conditions,it is found that the surface reactivity of SiH_3 is independent of the substrate temperature with beta=0.30+-0.03 whereas the silicon hydride composition on the a-Si:H surface changes drastically for increasing substrate temperature (from-SiH_3 to =SiH_2 to ident to SiH).The implications of these observations for the a-Si:H growth mechanism are addressed.
机译:我们报告了两项实验研究,以揭示对SIH_3基团与A-Si:H表面相互作用的洞察,如A-Si:H生长机制所必需的。A-Si对SiH_3的表面反应概率β :使用时间分辨腔振荡技术为基板温度(50-450degc)的函数来研究H.使用时间分离的腔振荡技术来研究沉积期间A-Si:H表面上的硅氢化硅-SiH_x。原位的组合衰减的总反射红外光谱和氩离子诱导的表面氢的解吸。对于SiH_3主导的等离子体条件,发现SiH_3的表面反应性与β= 0.30 + -0.03的基板温度无关,而硅A-Si的氢化物组合物:H表面急剧地改变用于将基板温度增加(从-SIH_3至= SiH_2到ident到SiH)。这些观察结果对A-Si:H生长机制是一个ddfressed。

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