Research output: Contribution to journal › Article › peer-review
N-doped titania nanoparticles containing Mo6 bromide and iodide clusters: Activity in photodegradation of rhodamine B and tetracycline. / Olawoyin, Christopher O.; Vorotnikov, Yuri A.; Asanov, Igor P. et al.
In: Chemosphere, Vol. 366, 143531, 16.10.2024.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - N-doped titania nanoparticles containing Mo6 bromide and iodide clusters: Activity in photodegradation of rhodamine B and tetracycline
AU - Olawoyin, Christopher O.
AU - Vorotnikov, Yuri A.
AU - Asanov, Igor P.
AU - Shestopalov, Michael A.
AU - Vorotnikova, Natalya A.
N1 - This work was supported by the Ministry of Science and Higher Education of the Russian Federation, No. 121031700321-3. We are grateful to the Microscopic Centre of the Siberian Branch of the Russian Academy of Sciences for granting access to the microscopic equipment.
PY - 2024/10/16
Y1 - 2024/10/16
N2 - Contamination of water sources is a major environmental problem with far-reaching consequences for humanity. Organic substances are among the most widespread and persistent pollutants. Advanced oxidation processes, especially photocatalysis, have been considered as one of the most promising technologies for organic pollution control. In this study, hybrid photocatalysts based on N-doped TiO2, which exhibits activity in the visible region of the spectrum, and different content of octahedral Mo6 bromide and iodide cluster complexes were synthesized to achieve the highest efficiency of the formed S-scheme photocatalytic system under white light irradiation. According to the data obtained, the resulting materials are nanoparticles with a diameter of ∼10 nm exhibiting absorption up to ∼550 nm. Photocatalytic studies were performed using model organic molecules – the more colored rhodamine B (RhB) and the less colored antibiotic tetracycline (TET). The most active samples showed high efficiencies against both pollutants with keff ∼0.3–0.4 and 0.4–0.5 min−1, respectively, while the activity of iodide complexes was ∼1.3 times higher than that of bromide complexes. The stability of the catalysts is preserved for up to 5 cycles of TET photodegradation.
AB - Contamination of water sources is a major environmental problem with far-reaching consequences for humanity. Organic substances are among the most widespread and persistent pollutants. Advanced oxidation processes, especially photocatalysis, have been considered as one of the most promising technologies for organic pollution control. In this study, hybrid photocatalysts based on N-doped TiO2, which exhibits activity in the visible region of the spectrum, and different content of octahedral Mo6 bromide and iodide cluster complexes were synthesized to achieve the highest efficiency of the formed S-scheme photocatalytic system under white light irradiation. According to the data obtained, the resulting materials are nanoparticles with a diameter of ∼10 nm exhibiting absorption up to ∼550 nm. Photocatalytic studies were performed using model organic molecules – the more colored rhodamine B (RhB) and the less colored antibiotic tetracycline (TET). The most active samples showed high efficiencies against both pollutants with keff ∼0.3–0.4 and 0.4–0.5 min−1, respectively, while the activity of iodide complexes was ∼1.3 times higher than that of bromide complexes. The stability of the catalysts is preserved for up to 5 cycles of TET photodegradation.
KW - N-doped titania
KW - Nanoparticles
KW - Octahedral halide molybdenum clusters
KW - Rhodamine B
KW - Tetracycline
KW - Rhodamines/chemistry
KW - Titanium/chemistry
KW - Iodides/chemistry
KW - Photolysis
KW - Catalysis
KW - Tetracycline/chemistry
KW - Nanoparticles/chemistry
KW - Bromides/chemistry
KW - Water Pollutants, Chemical/chemistry
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85206337361&origin=inward&txGid=b521d925322c2df6999e14d1b2c17977
UR - https://www.mendeley.com/catalogue/ac30150d-8a85-33c3-9c0e-a63289e84a41/
U2 - 10.1016/j.chemosphere.2024.143531
DO - 10.1016/j.chemosphere.2024.143531
M3 - Article
C2 - 39401674
VL - 366
JO - Chemosphere
JF - Chemosphere
SN - 0045-6535
M1 - 143531
ER -
ID: 60793669