Dengwei Yan , Fengyue Sun , Yanwei Ju , Haoping Di , Changle Yue , Yanfei Chen , Chongzheng Xu , Yukun Lu
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引用次数: 0
Abstract
The rational modulation of bimetallic intimately synergistic unsupported catalysts is the essential approach for efficient hydrodesulfurization (HDS). Herein, we have successfully produced NiMoS hollow spheres (H-NiMoS) by the Ni-MOF-engaged strategy using Ni metal–organic framework (Ni-MOF) as a precursor. The Ni-MOF serves as a landing site for vertically oriented MoS2 nanosheets and also acts as a nickel promoter for inducing the formation of the NiMoS active phase. The H-NiMoS catalyst achieves three-dimensional self-assembly of MoS2 nanosheets on hollow spheres, displaying a higher specific surface area (105 m2·g−1) compared to pure MoS2 (52 m2·g−1). The H-NiMoS catalyst produces vertical MoS2 with low stacking number (2–3 layers) and short slab length (2–4 nm), thus providing a large number of “rim” sites for HDS reaction. As expected, the H-NiMoS catalyst exhibits efficient HDS activity with 99.8 % conversion of dibenzothiophene (DBT) and 93.0 % conversion of 4,6-dimethyldibenzothiophene (4,6-DMDBT), as well as HDS selectivity that SHYD/DDS(DBT) = 1.3 and SHYD/DDS(4,6-DMDBT) = 3.2. Consequently, the Ni-MOF-engaged strategy of fabricating MoS2 nanosheets with vertically oriented structures by using Ni-MOF precursors provides significant guidance for improving the activity and HYD selectivity of conventional HDS catalysts by exposing more “rim” sites.
期刊介绍:
The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.