Single-atom Pt promotion of industrial Co-Mo-S catalysts for ultra-deep hydrodesulfurization

[Display omitted] •Pt-Co-Mo-S catalyst with up to 50% higher HDS activity than Co-Mo-S.•Pt single-atoms attached to corner and edge sites of Co-Mo-S nanostructures.•Pt is proposed to increase abundance of coordinatively undersaturated sites (CUS). We introduce a tertiary transition metal sulfide nan...

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Veröffentlicht in:Journal of catalysis 2021-11, Vol.403, p.74-86
Hauptverfasser: Weise, Christian Frederik, Falsig, Hanne, Moses, Poul Georg, Helveg, Stig, Brorson, Michael, Hansen, Lars Pilsgaard
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Sprache:eng
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Zusammenfassung:[Display omitted] •Pt-Co-Mo-S catalyst with up to 50% higher HDS activity than Co-Mo-S.•Pt single-atoms attached to corner and edge sites of Co-Mo-S nanostructures.•Pt is proposed to increase abundance of coordinatively undersaturated sites (CUS). We introduce a tertiary transition metal sulfide nanostructure, Pt-Co-Mo-S, for catalytic hydrodesulfurization (HDS) of sulfur-containing molecules in crude oil distillates with the aim to produce ultra-low sulfur transport fuels. The addition of ppm-levels of Pt to a standard industrial Co-Mo-S catalyst boosts the HDS activity by up to 46%. The promotional effect is examined by combining atomic-resolution Scanning Transmission Electron Microscopy (STEM), Energy Dispersive X-ray Spectroscopy (EDX), X-ray Absorption Near Edge Spectroscopy (XANES) and Density Functional Theory (DFT). It is shown that the Pt-Co-Mo-S catalyst contains predominantly single-layer MoS2 nanocrystals with Co atoms fully covering the S-edge terminations and Pt atoms uniquely attached to corner and edge sites in a platinum(IV) sulfide-like structural motif. Platinum is suggested to reduce the sulfur binding energy and increase the abundance of coordinately undersaturated sites (CUS) and not necessarily changing the reactivity towards 4,6-DMDBT molecules, although more elaborate studies are needed to address this in detail.
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2021.03.008