Infrared and Raman studies on Snx–Sb5–Se95−x chalcogenide glasses

• Published in: Journal of King Saud University. Science Vol. 21; no. 2; pp. 93 - 97
• Main Author: Adam, Abdallah Belal
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.07.2009
• Subjects: Raman; Sn–Sb–Se-chalcogenide glasses; IR; Raman; Sn–Sb–Se-chalcogenide glasses
• ISSN: 1018-3647
• DOI: 10.1016/j.jksus.2009.07.002

Tin–antimony–selenium (Sn–Sb–Se)-based systems belong to the ternary chalcogenide compounds of IV–V–VI group. They have potential applications in infrared region due to their heavy elemental masses, continuous variation of band gap-energies and lattice constants as well as electrical properties, with compositions. Structures of melt quench-synthesized samples of Snx–Sb5–Se95−x system, where x=0, 5, 10 and 12.5-mole% have been studied using Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy. FTIR spectra illustrates that addition of Sn-mole% to the system causes a shift in IR-peak’s intensity and width from long to the short wavelength. This change implies the breaking of Se chains that appeared around 210–254cm−1 and the occurrence of pyramidal SbSe3 around 147–210cm−1 and asymmetrical tetrahedral SnSe4 mode around 117–145cm−1 for Sn=5mole% up to 180cm−1 in Sn=12.5mole% spectra. Raman spectra show that a pyramidal SbSe3 peak is cited at 190-cm−1. The intensity of this peak is shifted towards −183cm−1 when Sn-mole% is added to the system. The results confirm the validity of using 4, 3 and 2 as co-ordination numbers of Sn, Sb and Se, respectively, in the amorphous region, which is contained by the average co-ordination number, μ⩽2.4 and the fraction of Sn–Se bonds, fSn–Se<44.3%.