CdTe and Related Compounds - Physics, Defects, etc., by R. Triboulet, et al.

By R. Triboulet, et al.

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E. I. Verlan, Zhurnal Prikladnoi Spektroskopii 21 (1974) 96–104 (in Russian). [35] S. S. Kim, P. Becla, Phys. Rev. B 43 (1991) 6598–6601. S. Vinogradov, Sov. Phys. Solid State 11 (1970) 2062–2071. [37] W. J. Y. Y. Zhang, Y. L. C. Shen, W. Giriat, Phys. Stat. Solidi (b) 147 (1988) 767–778. [38] S. Venugopalan, A. R. K. Ramdas, S. Rodriguez, Phys. Rev. B 25 (1982) 2681–2696. P. K. Vodopyanov, R. Triboulet, Solid State Comm. 45 (1983) 383–385. P. K. Vodopyanov, R. Triboulet, Phys. Rev. B 58 (1998) 1374–1384.

The conditions given earlier [44] are not valid for ternary alloys of the CdTe compounds [8, 9]. For example, the two-mode behavior occurs in the CdTe1ÀxSex crystal [34] while the conditions [44] predict an one-mode behavior, since the Se atom mass is greater than the reduced mass of elements of CdTe (mSe > mCdTe). The CdTe1ÀxSex reflection spectra show two Reststrahlen bands [34]. The intensity of the low-frequency band decreases continuously from a value of pure CdTe (x ¼ 0) to zero at x ! 1 whereas the intensity of the high-frequency band increases with the Se concentration.

Radisavljevic, J. Opt. Soc. Am. 57 (1967) 1475–1476. M. D. Rawcliffe, Appl. Opt. 7 (1968) 213. J. H. Sherman, R. Weil, Appl. Opt. 8 (1969) 1667–1671. A. Vinogradov, The study of optical phonons in AIIBVI compounds by far-infrared spectroscopy, Diss. D. (in Russian), Moscow Institute for Physics and Technology, 1973. K. A. Vinogradov, Crystal Lattice Defects 5 (1974) 125–136. K. A. V. A. Mityagin, Sov. Phys. Solid State 16 (1974) 912–915. [11] S. H. Thorland, Phys. Rev. B 9 (1974) 545–550. [12] A.

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