Structure of plasma-deposited amorphous hydrogenated boron-carbon thin films

被引:33
作者
Annen, A [1 ]
Sass, M [1 ]
Beckmann, R [1 ]
von Keudell, A [1 ]
Jacob, W [1 ]
机构
[1] EURATOM, Max Planck Inst Plasmaphys, D-85748 Garching, Germany
关键词
boron-carbon thin films; plasma deposition; ion-beam analysis;
D O I
10.1016/S0040-6090(97)00735-9
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Amorphous hydrogenated boron-carbon (a-B(1-x)C(x):H) thin films were prepared by radio-frequency plasma deposition using CH(4) and B(2)H(6) diluted in H(2) as precursor gases. The composition and density were determined by ion-beam analysis. The densities of the a-B:H and a-C:H films are similar with rho congruent to 1.72 g cm(-3), a value typical of hard and dense a-B:H and a-C:H films. Ternary a-B(1-x)C(x):H films are less dense, having a minimum density of rho congruent to 1.48 g cm(-3) at x = 0.71. Fourier transform infrared spectroscopy was used for qualitative and quantitative analysis of the bonding structures. The properties of films up to x approximate to 0.2 are comparable to those of pure a-B:H films. However, small carbon contents influence the film structure, mainly reducing the number of B-H-B bridge bonds, which are abundant in pure a-B:H films. Low film densities at x = 0.5 to 0.8 correlate with the maximum intensity of the extrinsic B-C vibrational mode around 1200 cm(-1) due to terminal -CH(3), groups indicating a less cross-linked network structure. Modifications of the network are indicated for x > 0.7. Below, carbon is predominantly sp(3) hybridised and bonded between boron neighbours. Above x = 0.7 the network becomes carbon dominated with an increasing number of carbon-carbon bonds and an increasing fraction of sp(2) hybridised carbon was observed. The extrinsic B-C vibrational mode at 1200 cm(-1) and the intrinsic B-C network vibration at 1500 cm(-1) were quantified over the whole range of a-B(1-x)C(x):H film compositions. The absorption constant of the extrinsic B-C vibrational mode at 1200 cm(-1) was estimated. (C) 1998 Elsevier Science S.A.
引用
收藏
页码:147 / 155
页数:9
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