A Raman and far‐infrared investigation of phonons in the rhombohedral V₂–VI₃ compounds Bi₂Te₃, Bi₂Se₃, Sb₂Te₃ and Bi₂(Te_1−<i>x</i>Se_<i>x</i>)₃ (0 &lt; <i>x</i> &lt; 1), (Bi_1−<i>y</i>Sb_<i>y</i>)₂Te₃ (0 &lt; <i>y</i> &lt; 1)

Abstract

Abstract The Raman‐active lattice vibrations of Bi 2 Se 3 , Bi 2 Te 3 , Sb 2 Te 3 , and their solid slutions, whose symmetries correspond to the R 3 m space group, are investigated by Raman scattering. Three of the four expected Raman modes, E g and A 1g , could be determined. The FIR optical properties of Bi 2 Te 3 crystal surfaces of improved quality ( E ∥ c and E ⟂ c ) and Bi 2 Se 3 ( E ⟂ c ) are re‐examined near helium and room temperature with a Fourier spectrometer, allowing a determination of the infrared‐active mode frequencies with higher accuracy. The results for Bi 2 Te 3 are compared to the predicted frequencies from the lattice dynamical model, given by Jenkins et al. The frequncy shifts of the Raman‐active modes in the mixed crystals show single‐mode and two‐mode behaviour, which is in agreement with simple models for the substitution of antimony and selenium atoms for bismuth and tellurium, respectively, in Bi 2 Te 3 .