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We present an experimental investigation of the temperature dependence of the TO-phonon mode frequencies for the HgTe-based II-VI semiconductor solid solutions. In the case of the ternary Hg0.9Zn0.1Te solid solution was shown a discontinuity in the temperature dependence of the HgTelike T0-mode and of the ZnTe-like T1-mode, similar to the Hg0.85Cd0.15Te system [Sheregii et al., Phys. Rev. Lett. 102, 045504 (2009)]. A generalization of the theoretical temperature shift of the phonon mode frequency as analytic equation is derived that includes both the anharmonic contribution and the electron-phonon e-p interaction which in this case is returnable--the electron subsystem effect on the phonon one. Data show that our equation satisfactorily describes the temperature shift of both Hg0.85Cd0.15Te and Hg0.90Zn0.10Te containing Dirac point (Eg ≡ Γ6 - Γ8=0) although one of the two constants describing the anharmonic shift of the HgTe-like mode should be positive what is abnormal too. In the case of the Hg0.80Cd0.20Te and Hg0.763Zn0.237Te solid solution, the role of the returnable e-p contribution is negligible but a positive temperature shift for the HgTelike modes occurs. This result does not allow to explain the positive temperature shift of these modes merely by the contribution of the (e-p) interaction. Indeed, the relativistic contribution to the chemical bonds induces an abnormal temperature shift of the electron states in Hg-based semiconductors - the effect is expected since the Hg d spin-orbit split contribution to chemical bonds may lead to an abnormal temperature shift of the HgTe-like modes. [ABSTRACT FROM AUTHOR]

This work presents far-infrared reflectivity spectra collected with synchrotron radiation on specially prepared CdTe monocrystals in the temperature region of 30–300 K. The investigated samples were of three different types characterized by the three different levels of hydrogenation—strong, middle, and low ones. In order to interpret the experimental data, the imaginary part of the dielectric function was evaluated by means of Kramers-Kronig transformation. To determine quantitatively the influence of hydrogen atoms on the phonon and vibrational spectra of hydrogenated CdTe crystals we used the special statistical model proposed in this paper. This model takes into account the tetrahedron as the basic structural unit and distinguishes the contribution of the hydrogen-bearing tetrahedra from the contribution of the hydrogen-free ones to the crystal phonon spectra. [ABSTRACT FROM AUTHOR]