Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Highly Defective Dark TiO2 Modified with Pt: Effects of Precursor Nature and Preparation Method on Photocatalytic Properties. / Fakhrutdinova, E. D.; Reutova, O. A.; Bugrova, T. A. и др.
в: Transactions of Tianjin University, Том 30, № 2, 04.2024, стр. 198-209.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Highly Defective Dark TiO2 Modified with Pt: Effects of Precursor Nature and Preparation Method on Photocatalytic Properties
AU - Fakhrutdinova, E. D.
AU - Reutova, O. A.
AU - Bugrova, T. A.
AU - Ovsyuk, I. Yu
AU - Kibis, L. S.
AU - Stonkus, O. A.
AU - Vasilchenko, D. B.
AU - Vodyankina, O. V.
AU - Svetlychnyi, V. A.
N1 - The authors thank Dr. M. A. Salaev for the language review. The HR TEM experiments were carried out using the facilities of the shared research center “National Center of Investigation of Catalysts” at Boreskov Institute of Catalysis. This work was funded by the Russian Science Foundation (No. 19-73-30026).
PY - 2024/4
Y1 - 2024/4
N2 - The study focused on the modification with platinum of dark defective titania obtained via pulsed laser ablation. Both the method of Pt introduction and the nature of the Pt precursor were varied. All samples exhibited similar phase compositions, specific surface areas, and Pt contents. High-resolution transmission electron microscopy coupled with pulsed CO adsorption revealed increased dispersity when photoreduction and the hydroxonitrate complex (Me4N)2[Pt2(OH)2(NO3)8] were used. The sample featured a high content of single-atom species and subnano-sized Pt clusters. The X-ray photoelectron spectroscopy results showed that the photoreduction method facilitated the appearance of a larger number of Pt2+ states, which appeared owing to the strong metal–support interaction (SMSI) effect of the transfer of electron density from the electron-saturated defects on the TiO2 surface to Pt4+. In the hydrogen evolution reaction, samples with a significant fraction of the Pt2+ ionic component, capable of generating short-lived Pt0 single-atom sites under irradiation due to the SMSI effect, exhibited the highest photocatalytic activity. The 0.5Pt(C)/TiO2–Ph sample exhibited the highest hydrogen yield with a quantum efficiency of 0.53, retaining its activity even after 8 h of operation.
AB - The study focused on the modification with platinum of dark defective titania obtained via pulsed laser ablation. Both the method of Pt introduction and the nature of the Pt precursor were varied. All samples exhibited similar phase compositions, specific surface areas, and Pt contents. High-resolution transmission electron microscopy coupled with pulsed CO adsorption revealed increased dispersity when photoreduction and the hydroxonitrate complex (Me4N)2[Pt2(OH)2(NO3)8] were used. The sample featured a high content of single-atom species and subnano-sized Pt clusters. The X-ray photoelectron spectroscopy results showed that the photoreduction method facilitated the appearance of a larger number of Pt2+ states, which appeared owing to the strong metal–support interaction (SMSI) effect of the transfer of electron density from the electron-saturated defects on the TiO2 surface to Pt4+. In the hydrogen evolution reaction, samples with a significant fraction of the Pt2+ ionic component, capable of generating short-lived Pt0 single-atom sites under irradiation due to the SMSI effect, exhibited the highest photocatalytic activity. The 0.5Pt(C)/TiO2–Ph sample exhibited the highest hydrogen yield with a quantum efficiency of 0.53, retaining its activity even after 8 h of operation.
KW - Dark (black) TiO2
KW - Hydrogen evolution reaction
KW - Photocatalysis
KW - Platinum reduction method
KW - Precursor type
KW - Pulsed laser ablation
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85189360144&origin=inward&txGid=59fef7cc04ed46d78ba8e66af5652e67
UR - https://www.mendeley.com/catalogue/bb52aa95-6a00-39bc-9820-67ba339b121a/
U2 - 10.1007/s12209-024-00388-z
DO - 10.1007/s12209-024-00388-z
M3 - Article
VL - 30
SP - 198
EP - 209
JO - Transactions of Tianjin University
JF - Transactions of Tianjin University
SN - 1006-4982
IS - 2
ER -
ID: 61079520