4.8 Article

MoS2 nanocrystals embedded in hierarchical hollow carbon microspheres for efficient aerobic oxidative desulfurization

Journal

MATERIALS TODAY CHEMISTRY
Volume 26, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.mtchem.2022.101197

Keywords

Dibenzothiophene; Aerobic oxidation; Molybdenum disulfide; Self assembly; Oxygen activation

Funding

  1. National Natural Science Foundation of China [21808098]
  2. Natural Science Foundation of Shandong Province [ZR2019QB025]
  3. Yantai Science and Technology Development Program [2019XDHZ106]
  4. Key Specialized Research and Development Breakthough (Science and Technology) in Henan Province [212102210214]

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This study reports a self-assembly approach to anchor MoS2 nanocrystals into hierarchical hollow carbon microspheres for efficient aerobic oxidative desulfurization (AODS) reactions. Experimental and theoretical calculations demonstrate that MoS2 nanocrystals exhibit highly active edge sites, which can effectively activate oxygen and adsorb sulfides, leading to extraordinary catalytic performance. Moreover, the carbon material ensures the chemical stability and persistence of the catalyst's activity.
Aerobic oxidative desulfurization (AODS) is an emerging sustainable technology for deep desulfurization of petroleum fuels, which requires robust catalysts to boost the efficient aerobic oxidation of thiophenes. Here we report a self-assembly approach to anchor homogeneously dispersed MoS2 nanocrystals into hierarchical hollow carbon microspheres for the efficient AODS of thiophenic sulfides. We show that MoS2 nanocrystals are vertically embedded in carbon nanosheets with highly active edge sites exposed to the surface, which could activate the aerobic oxidation of dibenzothiophene at 100 degrees C, and achieves a turnover frequency of 7.53 h-1, higher than that of the reported metallic oxide catalysts. Through a combination of experimental research and theoretical calculations, we demonstrate that the Mo edge of MoS2 can effectively activate oxygen and strongly adsorb sulfides, which endows our catalyst with extraordinary performance. Moreover, the close coupling of MoS2 nanocrystals in carbon ensures their chemical stability, so that the catalyst maintains unattenuated activity and unchanged chemical structure over seven repeated uses. This work provides both fundamental and practical insights in the design of efficient and stable nanocrystal-based catalysts.(c) 2022 Elsevier Ltd. All rights reserved.

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