Abstract
Accurate comparative measurements have been made of the X-ray diffraction pattern of a bulk arsenic sulphide glass prepared from the melt and a 250 μm film prepared by vapour deposition of the evaporated bulk. By using Ag Kα radiation, measurements have been made up to Q = 21 A ̊ −1 (Q = 4π sin θ/λ) so as to give good spatial resolution. Significant differences are found between bulk and film specimens, and in particular a shoulder is found on the high r side of the first peak in the distribution function for the film. Also, the film is richer in arsenic than the parent bulk. The results are compared in detail with a number of models, all of which involve covalent bonding requirements being fully satisfied, and it is concluded that there are more AsAs bonds in the film than the minimum required by stoichiometry and that a significant fraction ( ≈ 2 3 ) of these are unusually long ( ≈2.6 A ̊ compared to the more usual 2.5 Å). The most probable explanation is that the vapour contains a significant fraction of As 4S 4 species (in which the AsAs distances are ≈2.6 A ̊ ) and that the film contains a mixture of molecular species which have undergone considerable polymerization. The extent to which this results in a sheet-like structure similar to that proposed for the bulk glass remains unclear.
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