1981
DOI: 10.1002/pssb.2221050132
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Far Infrared and Raman Optical Study of α‐ and β‐In2S3 Compounds

Abstract: The far infrared spectra are investigated of cubic wIn,S, and tetragonal P-In,S, for E _L c and E I I e configurations for samples obtained after quenching and also after a long period of annealing.The quenched samples show a high reflectivity in the low frequency range, which disappears after annealing. Also for ci-In,S, a greater number of bands appears after annealing. A large number of' peaks are also observed in light scattering, which are concentrated in the same narrow frequency range, as in the infrare… Show more

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Cited by 103 publications
(44 citation statements)
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References 17 publications
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“…Assuming that all peaks correspond to a first-order spectrum, the frequency at which each of them occurs would correspond to a normal mode of vibration. Fifteen normal modes of vibrations are thus observed, which correspond exactly to those given by a sample of b-In 2 S 3 with unpolarized light (36). The small change of peak intensity and the instability of baseline are due to the influence of fluorescence.…”
Section: Raman Spectrummentioning
confidence: 83%
“…Assuming that all peaks correspond to a first-order spectrum, the frequency at which each of them occurs would correspond to a normal mode of vibration. Fifteen normal modes of vibrations are thus observed, which correspond exactly to those given by a sample of b-In 2 S 3 with unpolarized light (36). The small change of peak intensity and the instability of baseline are due to the influence of fluorescence.…”
Section: Raman Spectrummentioning
confidence: 83%
“…Sample B-CIS1 exhibits two broad peaks at 130 cm -1 and 302 cm -1 whereas single peak is obtained in sample B-CIS3 at 285 cm -1 . An intense mode at ~302 cm -1 in sample B-CIS1 has been previously noticed for indium rich CuInS 2 samples [15,[16][17] and β-In 2 S 3 presents a strong peak close to 302 cm -1 with A 1 symmetry [18]. Raman peak is observed at 285 cm -1 corresponds to the symmetric A 1 mode (pure anion vibration) of the sulphur lattice and found to be dominating Raman mode in device-quality CuInS 2 material [19].…”
Section: Micro-raman Measurementsmentioning
confidence: 59%
“…According to EXAFS studies, In-In homopolar bonds are less probable being the expression of the absence of indium cluster with the respect of chemical order even for metal-metal bonding [14]. Nevertheless, this wide band centred at 242 cm À1 has also been related to the presence of [InS 6 ] octahedral sites [15,16] due to the presence of two really intense bands at 242 cm À1 and 308 cm À1 betaIn 2 S 3 spinel-like structure where In atoms occupy octahedral and a part of tetrahedral sites [22]. Due to the increase of In/Ge ratio with the gradual introduction of CsI in the binary sample, the expected decrease of the bands in the range of 340-430 cm À1 related to the vibrations of the [GeS 4 ] entities is observed.…”
Section: Raman Spectroscopymentioning
confidence: 98%