Synthesis and characterization of temperature-dependent nanospherical Cu2−xSe thin films for photoelectrochemical cell application

In this investigation, copper selenide (Cu 2− x Se, x  = 0.57) thin films were synthesized employing the environmentally benign self-organized arrested precipitation technique (APT) on the soda-lime glass (SLG) as well as on tin-doped indium oxide (ITO) substrates, varying deposition temperatures of...

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Published inJournal of materials science. Materials in electronics Vol. 35; no. 28; p. 1836
Main Authors Kalvikatte, Pratik M., Patil, P. R., Mahadik, V. M., Mayanekar, A. A., Dongale, T. D., Mane, R. M., Bhosale, P. N., Khot, Kishorkumar V.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.10.2024
Springer Nature B.V
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Summary:In this investigation, copper selenide (Cu 2− x Se, x  = 0.57) thin films were synthesized employing the environmentally benign self-organized arrested precipitation technique (APT) on the soda-lime glass (SLG) as well as on tin-doped indium oxide (ITO) substrates, varying deposition temperatures of 40 °C, 55 °C, 70 °C. Characterization, encompassing UV–Vis spectrophotometry, X-ray diffraction (XRD), and scanning electron microscopy (SEM) with energy-dispersive spectroscopy (EDS). The results elucidated distinctive attributes of the thin films, having a notably visible light absorption profile in the range of 600–700 nm for all samples and characterized by bandgap energy of 1.59 eV for the sample at 70 °C. The manifestation of a singularly phase-pure cubic crystal structure for temperature of 70 °C and hexagonal for 45 °C and 55 °C temperatures, and the emergence of nanospherical surface morphology. Significantly, the Cu 2− x Se thin films evinced augmented photoelectrochemical (PEC) proficiency, prolonged stability in PEC environments, and exhibited consistent p-type conductivity. Underscoring their prospective utility in energy conversion, particularly in the context of photoelectrochemical cells.
ISSN:0957-4522
1573-482X
DOI:10.1007/s10854-024-13592-3