Authors
Jing Cao, Kejun Chen, Tianyi Liu, Jialing Liu, Cen Zhang
Published in
Inorganic chemistry. Jul 01, 2026. Epub Jul 01, 2026.
Abstract
Layer-controlled synthesis of MoS2 is of great importance to understanding the structure-performance relation in the hydrodeoxygenation (HDO) reaction. However, the traditional chemical exfoliation method suffers from the disadvantages of a low yield and complex operation. Herein, we report a simple strategy to achieve layer-controllable synthesis of MoS2 by thermal decomposition of alkylammonium thiomolybdates. Through increasing the length of the alkyl chain, the layer number of MoS2 is tuned from multilayer to monolayer due to the obstruction effect of amorphous carbon in the growth process. Adopting 4-methylphenol (4-MP) as a probe molecule, it is found that the intrinsic HDO activity and direct deoxygenation (DDO) selectivity are enhanced with the decrease of the stacking number of MoS2 catalysts. Consequently, the monolayer MoS2-Bu prepared by thermal decomposition of tetrabutylammonium thiomolybdate shows the highest 4-MP conversion and toluene selectivity. By further doping Co promoters to form Co-Mo-S active phase, the Co/MoS2-Bu catalyst achieved 99.6% 4-MP conversion and 99.3% toluene selectivity at 220 °C and 3.0 MPa for steady running of 48 h. The excellent stability is attributed to the isolation and hydrophobic effect of carbon species, which prevent the monolayer MoS2 particles from sintering and surface oxidation.
PMID:
42385176
Bibliographic data and abstract were imported from PubMed on 02 Jul 2026.
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