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The structural ordering of thin silicon films at the amorphous to nano-crystalline phase transition by GISAXS and Raman spectroscopy

机译:GISAXS和拉曼光谱在非晶相到纳米晶相变过程中薄膜的结构排序

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摘要

Thin silicon films were deposited by the plasma-enhanced chemical vapour deposition method using microwave (MW) and standard radio frequency (RF) gas discharge in silane gas diluted by hydrogen in the range that produces a mixture of amorphous and crystalline phases. The samples were analysed by Raman spectroscopy and grazing incidence small-angle X-ray scattering (GISAXS), while the threshold for the transition between the amorphous and crystalline phase was checked by the change in electrical conductivity. The crystalline fraction, estimated by Raman spectroscopy, varied between 0% and 70% while the individual crystal sizes were between 3 and 9 nm. However, the size distribution was broad suggesting also the existence of smaller and larger crystals. The "particles" observed by GISAXS, most probably voids, were in the range between 2 and 12 nm. The voids in samples deposited by MW plasma were larger when closer to the surface. Their shape indicated the formation of a columnar structure perpendicular to the surface, more pronounced at higher temperature. The samples deposited by RF plasma and low power had spherically symmetric "particles" with uniform size across the depth of the samples. An increase of the RF power resulted in the formation of a columnar structure parallel to the surface. The observed differences are discussed in relation to the difference in growing kinetics of the used deposition methods.
机译:通过等离子体增强化学气相沉积法沉积硅薄膜,该方法使用微波(MW)和标准射频(RF)气体在氢稀释的硅烷气体中产生一定范围的非晶和结晶相的混合物进行放电。通过拉曼光谱和掠入射小角X射线散射(GISAXS)分析样品,同时通过电导率变化检查非晶相和结晶相之间转变的阈值。通过拉曼光谱法估计的晶体分数在0%至70%之间变化,而单个晶体尺寸在3至9nm之间。但是,尺寸分布很宽,表明也存在越来越小的晶体。 GISAXS观察到的“颗粒”(很可能是空隙)在2至12 nm之间。当接近表面时,MW等离子体沉积的样品中的空隙更大。它们的形状指示出垂直于表面的柱状结构的形成,在较高温度下更明显。通过RF等离子体和低功率沉积的样品具有球形对称的“颗粒”,在整个样品深度上尺寸均一。 RF功率的增加导致形成平行于表面的柱状结构。讨论了所观察到的差异,涉及所用沉积方法的生长动力学差异。

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