4.7 Article

Ce-doped MIL-125-NH2 coupled Ce4+/Ce3+and Ti4+/Ti3+redox mediators for thermo-enhanced photocatalytic oxidative desulfurization

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CHINESE CHEMICAL LETTERS
卷 34, 期 5, 页码 -

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2022.107766

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Photocatalytic oxidative desulfurization; Ce-doped-MIL-125-NH 2; Ce 4+; Ce 3+andTi 4+; Ti 3+redox couples; Thermal enhancement; Visible light; Photocatalytic oxidation

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Photocatalytic oxidative desulfurization (PODS) using efficient Ce-doped MIL-125-NH2 photocatalysts was successfully achieved for the removal of dibenzothiophene (DBT) under mild reaction conditions. The high performance was attributed to the high surface area and the formation of Ce-Ti-oxo clusters, as well as the valence transformation of Ce4 + /Ce3 + and Ti4 + /Ti3 + redox mediators. Increasing the reaction temperature was found to enhance the PODS performance, and a thermo-enhanced PODS mechanism was proposed.
Photocatalytic oxidative desulfurization (PODS) over efficient earth-abundant catalysts to obtain clean fuel oil is of great importance for the environmental protection. In this work, a series of Ce-doped MIL-125-NH2 photocatalysts were successfully prepared via a simple in-situ doping method and exhibited superior PODS performance of dibenzothiophene (DBT) under mild reaction conditions. The 1.0 mol% Ce/MIL-125-NH2 catalyst achieved 100% sulfur removal within 22 min at 30 degrees C under visible light illumination, which is mainly attributed to the high surface area and the formation of Ce-Ti-oxo clusters due to electronic coupling. The valence transformation of Ce4 + /Ce3 + and Ti4 + /Ti3 + redox mediators could not only expose abundant Lewis acid sites, but also promote the separation and transfer of photogenerated charges. In addition, increasing the reaction temperature has been demonstrated to be effective in promoting the PODS performance. Additionally, a thermo-enhanced PODS mechanism was proposed over Ce/MIL-125-NH2, demonstrating the great potential of thermal energy to promote the desulfurization activity.(c) 2023 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.

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