Please use this identifier to cite or link to this item: https://idr.nitk.ac.in/jspui/handle/123456789/16740
Title: ZnxSn1-xS thin films: A study on its tunable opto-electrical properties for application towards a high efficient photodetector
Authors: Barman B.
Bangera K.V.
Shivakumar G.K.
Issue Date: 2020
Citation: Solar Energy Vol. 206 , , p. 479 - 486
Abstract: Zinc sulfide (ZnS) and tin sulfide (SnS) are crucial semiconductors with potential use in various opto-electronic applications. By incorporating ZnS and SnS to form ZnxSn1-xS thin film, one can expect exceptional opto-electrical properties due to their large band gap dissimilarity. Herein, thin films of ZnxSn1-xS (0.0 ≤ x ≤ 1.0) were successfully deposited on glass substrates using a thermal evaporation method for the first time and its various properties were analyzed. X-ray diffraction (XRD) analysis confirmed the polycrystalline behavior of ZnxSn1-xS films with a preferred orientation along the (1 1 1) plane. The absence of any secondary peaks along with the shift in the (1 1 1) peak position to lower 2θ values with increasing Zn concentration confirmed the formation of a solid solution. SEM analysis depicted the presence of uniform and homogeneous films. The formation of nearly stoichiometric ZnxSn1-xS films was verified using an energy dispersive spectroscopy (EDS). The electrical and optical properties of the films were estimated from the two-probe method and UV–Vis spectroscopy, respectively. The energy band gap values decreased from 3.49 eV to 1.54 eV as the composition of the ZnxSn1-xS films was varied. The various opto-electrical parameters were investigated and the photosensitivity was found highest at 43.38 for the Zn0.10Sn0.90S films. The observed tunable opto-electrical properties of the ZnxSn1-xS films suggests that the films can be utilized for a wide range of opto-electronic applications. © 2020 International Solar Energy Society
URI: https://doi.org/10.1016/j.solener.2020.06.026
http://idr.nitk.ac.in/jspui/handle/123456789/16740
Appears in Collections:1. Journal Articles

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