Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/26996
Title: Optimization of growth parameters of electrodeposited tin oxide thin films for PV Applications
Authors: Kafi, F. S. B.
Gunaratne, B. H.
Jayathilaka, K. M. D. C.
Wijesundera, R. P.
Keywords: Electrodeposition, Photovoltaics, SnO2, Thin film, Tin oxide
Issue Date: 2023
Publisher: Faculty of Science, University of Kelaniya Sri Lanka
Citation: Kafi F. S. B.; Gunaratne B. H.; Jayathilaka K. M. D. C.; Wijesundera R. P. (2023) Optimization of growth parameters of electrodeposited tin oxide thin films for PV Applications, Proceedings of the International Conference on Applied and Pure Sciences (ICAPS 2023-Kelaniya) Volume 3, Faculty of Science, University of Kelaniya Sri Lanka. Page 191-197
Abstract: Tin oxide (SnO2) is a promising photoactive semiconducting material due to its optoelectronics properties. Even though, growth of SnO2 using the method of electrodeposition is advantageous, it has paved low attention among semiconductor researchers. In this study, well-adhered photoactive SnO2 thin film was successfully electrodeposited on Cu substrates. The growth parameters, such as film deposition potential, bath temperature, and duration of deposition were optimized. Electrodeposition of SnO2 layers was performed on copper substrates in a threeelectrode electrochemical cell using a solution containing 30 mM SnCl2 and 150 mM HNO3 at a deposition potential of -0.85 V vs. Ag/AgCl. The fabricated best thin film resulted JSC value of 410 �A cm-2 and VOC value of 113 mV in 0.1 M NaNO3 electrolyte. The best thin film obtained at a bath temperature of 85◦ C for a deposition time of 120 seconds. The Mott-Schottky analysis revealed that the fabricated SnO2 thin film exhibits n-type conductivity, and it has a flat band potential of -0.51 V vs. Ag/AgCl.
URI: http://repository.kln.ac.lk/handle/123456789/26996
Appears in Collections:ICAPS 2023

Files in This Item:
File Description SizeFormat 
ICAPS 2023 191.pdf617.85 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.