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 AsAs 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 AsAs 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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