Sriraman Saravanapriyan, Agarwal Sumit, Aydil Eray S, Maroudas Dimitrios
Department of Chemical Engineering, University of California, Santa Barbara, California 93106-5080, USA.
Nature. 2002 Jul 4;418(6893):62-5. doi: 10.1038/nature00866.
Hydrogenated amorphous and nanocrystalline silicon films manufactured by plasma deposition techniques are used widely in electronic and optoelectronic devices. The crystalline fraction and grain size of these films determines electronic and optical properties; the nanocrystal nucleation mechanism, which dictates the final film structure, is governed by the interactions between the hydrogen atoms of the plasma and the solid silicon matrix. Fundamental understanding of these interactions is important for optimizing the film structure and properties. Here we report the mechanism of hydrogen-induced crystallization of hydrogenated amorphous silicon films during post-deposition treatment with an H(2) (or D(2)) plasma. Using molecular-dynamics simulations and infrared spectroscopy, we show that crystallization is mediated by the insertion of H atoms into strained Si-Si bonds as the atoms diffuse through the film. This chemically driven mechanism may be operative in other covalently bonded materials, where the presence of hydrogen leads to disorder-to-order transitions.
通过等离子体沉积技术制造的氢化非晶硅和纳米晶硅薄膜广泛应用于电子和光电器件中。这些薄膜的晶体分数和晶粒尺寸决定了其电学和光学性质;决定最终薄膜结构的纳米晶成核机制受等离子体中的氢原子与固态硅基体之间相互作用的支配。对这些相互作用的基本理解对于优化薄膜结构和性质很重要。在此,我们报告了在使用H₂(或D₂)等离子体进行沉积后处理期间氢化非晶硅薄膜的氢诱导结晶机制。通过分子动力学模拟和红外光谱,我们表明,随着原子在薄膜中扩散,H原子插入应变的Si-Si键中介导了结晶过程。这种化学驱动机制可能在其他共价键合材料中起作用,在这些材料中,氢的存在会导致无序到有序的转变。