Daouahi Mohsen, Omri Mourad, Kerm Abdul Ghani Yousseph, Al-Agel Faisal Abdulaziz, Rekik Najeh
Physics Department, Faculty of Science, University of Hail, Saudi Arabia.
Physics Department, Faculty of Science, Aljouf University, Sakaka, Saudi Arabia.
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Feb 5;136 Pt C:1409-17. doi: 10.1016/j.saa.2014.10.029. Epub 2014 Oct 22.
The aim of the study reported in this paper is to investigate the role of the high partial pressure of hydrogen introduced during the growth of nanocrystalline silicon carbide thin films (nc-SiC:H). For this purpose, we report the preparation as well as spectroscopic studies of four series of nc-SiC:H obtained by radio-frequency magnetron sputtering at high partial pressure of hydrogen by varying the percentage of H2 in the gas mixture from 70% to 100% at common substrate temperature (TS=500°C). The effects of the dilution on the structural changes and the chemical bonding of the different series have been studied using Fourier transform infrared and Raman spectroscopy. For this range of hydrogen dilution, two groups of films were obtained. The first group is characterized by the dominance of the crystalline phase and the second by a dominance of the amorphous phase. This result confirms the multiphase structure of the grown nc-SiC:H thin films by the coexistence of the SiC network, carbon-like and silicon-like clusters. Furthermore, infrared results show that the SiC bond is the dominant absorption peak and the carbon atom is preferentially bonded to silicon. The maximum value obtained of the crystalline fraction is about 77%, which is relatively important compared to other results obtained by other techniques. In addition, the concentration of CHn bonds was found to be lower than that of SiHn for all series. Raman measurements revealed that the crystallization occurs in all series even at 100% H2 dilution suggesting that high partial pressure of hydrogen favors the formation of silicon nanocrystallites (nc-Si). The absence of both the longitudinal acoustic band and the transverse optical band indicate that the crystalline phase is dominant.
本文所报道研究的目的是探究在纳米晶硅碳化薄膜(nc-SiC:H)生长过程中引入的高氢分压所起的作用。为此,我们报告了通过射频磁控溅射在高氢分压下制备以及光谱研究的四个系列的nc-SiC:H,在常见衬底温度(TS = 500°C)下,将混合气体中H2的百分比从70%变化到100%。使用傅里叶变换红外光谱和拉曼光谱研究了稀释对不同系列结构变化和化学键合的影响。对于这个氢稀释范围,获得了两组薄膜。第一组的特征是晶相占主导,第二组的特征是非晶相占主导。这一结果通过SiC网络、类碳和类硅团簇的共存证实了生长的nc-SiC:H薄膜的多相结构。此外,红外结果表明SiC键是主要吸收峰,碳原子优先与硅键合。获得的最大结晶分数值约为77%,与通过其他技术获得的其他结果相比相对较高。另外,发现所有系列中CHn键的浓度都低于SiHn键的浓度。拉曼测量表明,即使在100% H2稀释下,所有系列中都发生了结晶,这表明高氢分压有利于硅纳米晶体(nc-Si)的形成。纵向声学带和横向光学带的缺失表明晶相占主导。