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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received September 23, 2024
Accepted December 25, 2024
Available online March 25, 2025
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Synthesis, Structural and Photocatalytic Behavior of Sn–F Co-Doped TiO 2 Nanomaterials

Faculty of Chemistry , Southern Federal University , Rostov-on-Don , Russia 1Institute of Physical and Organic Chemistry, Southern Federal University , Rostov-on-Don, 344090 , Russia 2Platov South-Russian State Polytechnic University (NPI) , Novocherkassk , Russia
Korean Journal of Chemical Engineering, March 2025, 42(3), 689-699(11)
https://doi.org/10.1007/s11814-024-00374-0

Abstract

of modifying agents (0.3–10 mol.% Sn 4+ and 0.3–10 mol.% F − ) and calcination temperature (500–800 °C) on the properties

of the resulting nanomaterials was studied. Nanomaterials were analyzed using X-ray diff raction, high-resolution transmission

electron microscopy, energy dispersive X-ray spectroscopy, selected area electron diff raction, diff erential scanning

calorimetric and thermogravimetric analyses, UV–visible diff use refl ectance spectroscopy and other methods. It was found

that the amounts of introduced Sn 4+ and F − ions and the temperature of the heat treatment regulate the phase composition and

particle size of the resulting nanomaterials, as well as adjust the photocatalytic properties of the materials to be activated by

UV and visible light. The materials are nanoscale, with an average size is 13–57 nm depending on the synthesis conditions.

The best photocatalytic performance was observed for a material containing 0.3 mol.% Sn 4+ and 0.6 mol.% F − . Co-doping

of TiO 2 with F − and Sn 4+ ions signifi cantly enhances the photocatalytic properties of TiO 2 in both visible and ultraviolet

ranges, owing to a decrease in the band gap.

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