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Room Temperature Growth of Hydrogenated Amorphous Silicon Films by Dielectric Barrier Discharge Enhanced CVD

机译:介质阻挡放电增强CVD法室温生长氢化非晶硅膜

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摘要

Hydrogenated amorphous silicon (a-Si: H) films were deposited on Si (100) and glass substrates by dielectric barrier discharge enhanced chemical vapour deposition (DBD-CVD) in (SiH4+H2) atmosphere at room temperature. Results of the thickness measurement, SEM (scanning electron microscope), Raman, and FTIR (Fourier transform infrared spectroscopy) show that with the increase in the applied peak voltage, the deposition rate and network order of the films increase, and the hydrogen bonding configurations mainly in di-hydrogen (Si-H2) and poly hydrogen (SiH2)n are introduced into the films. The UV-visible transmission spectra show that with the decrease in SiH4/ (SiH4+H2) the thin films' band gap shifts from 1.92 eV to 2.17 eV. These experimental results are in agreement with the theoretic analysis of the DBD discharge. The deposition of a-Si: H films by the DBD-CVD method as reported here for the first time is attractive because it allows fast deposition of a-Si: H films on large-area low-melting-point substrates and requires only a low cost of production without additional heating or pumping equipment.
机译:在室温(SiH4 + H2)下,通过电介质阻挡放电增强化学气相沉积(DBD-CVD),在硅(100)和玻璃基板上沉积氢化非晶硅(a-Si:H)膜。厚度测量,SEM(扫描电子显微镜),拉曼和FTIR(傅立叶变换红外光谱)的结果表明,随着施加的峰值电压的增加,薄膜的沉积速率和网络顺序增加,并且氢键构型增加将主要以二氢(Si-H 2)和多氢(SiH 2)n引入膜中。紫外可见透射光谱表明,随着SiH4 /(SiH4 + H2)的减少,薄膜的带隙从1.92 eV变为2.17 eV。这些实验结果与DBD放电的理论分析是一致的。如此处首次报道的那样,通过DBD-CVD方法沉积a-Si:H膜很有吸引力,因为它可以在大面积低熔点衬底上快速沉积a-Si:H膜,并且只需要生产成本低,无需额外的加热或抽水设备。

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