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Transpolyacetylene chains in hydrogenated amorphous carbon films free of nanocrystalline diamond

机译:氢化非晶碳膜中的反式聚乙炔链不含纳米晶金刚石

摘要

The microstructure of distributed electron cyclotron resonance plasma-deposited hydrogenated amorphous carbon films (a-C:H) was investigated using electron diffraction, Raman spectroscopy, and Fourier transform infrared spectroscopy. Experimental evidence of the existence of transpolyacetylene (TPA) chains in a-C:H films free of nanocrystalline diamond is presented. The values of the mean bond angles and lengths and first neighbor numbers are consistent with the TPA data. The Raman spectra were fitted using the G and D bands and the bands centered at 1140, 1233, and 1475 cm(-1) assigned to TPA chains modes. The relative intensity of the latter decreases while hydrogen content decreases. A significant sp(2)-CH olefinic mode contribution to the infrared stretching band is observed for the low-density films (similar to1.2 g/cm(3)). TPA chains growth is enhanced when ion current density and energy decrease. (C) 2003 American Institute of Physics. (DOI: 10.1063/1.1538349)
机译:使用电子衍射,拉曼光谱和傅里叶变换红外光谱研究了分布电子回旋共振等离子体沉积的氢化非晶碳膜(a-C:H)的微观结构。提出了在无纳米晶金刚石的a-C:H膜中存在反式聚乙炔(TPA)链的实验证据。平均键角和长度以及第一邻居数的值与TPA数据一致。使用G和D波段拟合拉曼光谱,并以1140、1233和1475 cm(-1)为中心将波段分配给TPA链模式。后者的相对强度降低,而氢含量降低。对于低密度薄膜(类似于1.2 g / cm(3)),观察到了对红外拉伸带的重要sp(2)-CH烯烃模式贡献。当离子电流密度和能量降低时,TPA链的生长会增强。 (C)2003美国物理研究所。 (DOI:10.1063 / 1.1538349)

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