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Elucidating the structural, morphological and optical properties of chalcogenide glasses within antimony-tin-selenium ternary system.

Authors :
Khajuria, Rajni
Singh, Anoop
Rather, Mehraj ud Din
Sharma, Anshu
Angotra, Poonam
Sundramoorthy, Ashok K.
Dixit, Saurav
Vatin, Nikolai Ivanovich
Arya, Sandeep
Source :
Applied Physics A: Materials Science & Processing. Oct2024, Vol. 130 Issue 10, p1-11. 11p.
Publication Year :
2024

Abstract

Antimony-Selenium-Tin (Sb-Se-Sn) is a ternary chalcogenide have wide range of potential applications, because of their high strength, various crystal lattices, and electrical characteristics. In this work, the melt quenching method was used to synthesize the nanoparticles of Sb14Se86-xSnx (x = 0, 3, 6, 9, 12) chalcogenide glasses. X-ray diffraction (XRD) and the Scanning electron microscopy (SEM) of the Sb14Se74Sn12 chalcogenide glasses ascertained the amorphous characteristics. No extra impurity was detected in any chalcogenide, and the presence of only Sb, Se and Sn was detected from the EDS spectra. The decrease in band gap is revealed with the increase of Sn content in the Sb14Se86-xSnx glasses. Lowest band gap was observed in the Sb14Se74Sn12 chalcogenide, attributed to the large crystallite size. The FTIR spectrum of the sample reveals an absorption band roughly between 500 –400 cm-1, attributed to the vibrational modes for Sb–Se, Sn–Se and Sn-Sb bonds. In the chalcogenide glasses, the Sn and Sb 3d state comprises of two peaks, corresponding to doublet state (3d5/2 and 3d3/2), while as Se has only singlet state (3d). In conclusion, in the Sb14Se86-xSnx (x = 12) chalcogenide glass, an increase in photoluminescence intensity and the decrease in band gap makes it potential candiate for the infrared detectors, and the infrared optical fibres. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09478396
Volume :
130
Issue :
10
Database :
Academic Search Index
Journal :
Applied Physics A: Materials Science & Processing
Publication Type :
Academic Journal
Accession number :
180370204
Full Text :
https://doi.org/10.1007/s00339-024-07876-y