Noble Metal-Free 2D 1T-MoS2 Edge Sites Boosting Selective Hydrogenation of Maleic Anhydride
Layered two-dimensional (2D) materials have attracted enormous attention as appealing catalysts and supports for various electro- and photocatalytic transformations. Here, we report another unique behavior of 2D MoS2 for heterogeneous selective hydrogenation, which exhibits excellent activity (100%)...
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Veröffentlicht in: | ACS catalysis 2022-08, Vol.12 (15), p.8986-8994 |
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creator | Zhao, Yi Chang, Kuan Gu, Qingqing Yang, Bing Xu, Jing Zhang, Ying Pan, Chengsi Wang, Zhenlin Lou, Yang Zhu, Yongfa |
description | Layered two-dimensional (2D) materials have attracted enormous attention as appealing catalysts and supports for various electro- and photocatalytic transformations. Here, we report another unique behavior of 2D MoS2 for heterogeneous selective hydrogenation, which exhibits excellent activity (100%) and selectivity (100%) for industrially important maleic anhydride (MAH) hydrogenation to succinic anhydride (SA), comparable to the cutting-edge commercial noble-metal catalysts. The specific reaction rate increases linearly with the concentration of 1T-phase MoS2, confirming the excellent intrinsic activity of 1T-MoS2 for MAH to SA. The electron-rich Mo sites on the oxidized Mo edges of 1T-MoS2 form a pocketlike active site (HO–Mo–S–Mo–S–Mo–OH), which confines the MAH adsorption mode due to the steric effect and further promotes H2 activation due to the itinerant electrons of Mo4+ in 1T-MoS2. The strategy of constructing edge-confined active centers with specific phase composition of 2D materials opens an approach to developing highly efficient catalysts for chemical transformations. |
doi_str_mv | 10.1021/acscatal.2c02122 |
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Here, we report another unique behavior of 2D MoS2 for heterogeneous selective hydrogenation, which exhibits excellent activity (100%) and selectivity (100%) for industrially important maleic anhydride (MAH) hydrogenation to succinic anhydride (SA), comparable to the cutting-edge commercial noble-metal catalysts. The specific reaction rate increases linearly with the concentration of 1T-phase MoS2, confirming the excellent intrinsic activity of 1T-MoS2 for MAH to SA. The electron-rich Mo sites on the oxidized Mo edges of 1T-MoS2 form a pocketlike active site (HO–Mo–S–Mo–S–Mo–OH), which confines the MAH adsorption mode due to the steric effect and further promotes H2 activation due to the itinerant electrons of Mo4+ in 1T-MoS2. 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Here, we report another unique behavior of 2D MoS2 for heterogeneous selective hydrogenation, which exhibits excellent activity (100%) and selectivity (100%) for industrially important maleic anhydride (MAH) hydrogenation to succinic anhydride (SA), comparable to the cutting-edge commercial noble-metal catalysts. The specific reaction rate increases linearly with the concentration of 1T-phase MoS2, confirming the excellent intrinsic activity of 1T-MoS2 for MAH to SA. The electron-rich Mo sites on the oxidized Mo edges of 1T-MoS2 form a pocketlike active site (HO–Mo–S–Mo–S–Mo–OH), which confines the MAH adsorption mode due to the steric effect and further promotes H2 activation due to the itinerant electrons of Mo4+ in 1T-MoS2. 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title | Noble Metal-Free 2D 1T-MoS2 Edge Sites Boosting Selective Hydrogenation of Maleic Anhydride |
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