We report on the composition dependence of thermal vibrations in Hg[in1- xZn x Te solid solutions ( x = 0.13,0.20, 0.50, 0.75) determined by X-ray diffraction at room temperature (297 K) and in some cases ( x = 0.50, 0.75) at 143 K. Although some ambiguity on the results obtained for x ≅ 0.50 cannot be avoided as being intrinsic to the problem, it is shown, by taking into account the results obtained by Cooper, Rouse and Fuess Acta crystallogr. A29, 1973 on ZnTe ( x = 1), that the conventional harmonic B factor ( B = 8 π 2〈 u 2〉 where 〈 u 2〉 is the mean-square displacement of the atom in any direction) of the average (HgZn) cation decreases almost linearly from B Hg- Zn = 2.82 ( σ = 0.09) Å2 to B jn = 1.296 ( σ = 0.034) Å 2 when x varies from x = 0.13 to x = 1. This is interpreted as resulting from the almost composition independent B Hg ≅ 2.7 Å 2 and B Hg ≌ 1.3 Å 2. By contrast the B factor of the Te anion exhibits a more complex behaviour varying in a non-monotonic way from 2.03 (σ = 0.07) Å 2 for x = 0.13 to 0.76 ( σ = 0.01) Å 2 for x = 1. In the alloys the B factors do not vary linearly with T between 297 and 143 K. It is shown that this is not attributable to quantum effects (zero point motion) but is due to a static structural disorder which affects the metal as well as the anion sublattices, the average atomic distortion being about 0.08 Å. The experimental data also show contributions arising from third-order anharmonic thermal vibrations of the atoms.
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