Ayesha Shafiq , Iryna Danylo , Lukas Kolacny , Berke Sevemez , Jan Luxa , Martin Vesely , Martina Pitinova
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引用次数: 0
Abstract
The selective hydrogenation of cinnamaldehyde (CAL), a model α,β-unsaturated aldehyde, yields valuable products such as cinnamyl alcohol (COL) and hydrocinnamaldehyde (HCAL). Pt-based catalysts supported on transition metal dichalcogenides (MoS2, WS2, and their composite) in bulk forms and their exfoliated counterparts were synthesized using microwave-assisted and wet impregnation methods. Characterization (SEM/EDS, TEM, XRF, XRD, and BET) confirmed ∼9 wt% Pt loading, preserved layered structures, and well-dispersed nanoparticles. Catalysts based on 2D supports provided finer Pt dispersion (2–6 nm), with microwave synthesis yielding smaller, more uniform particles, especially in the Mo–W composite. Catalytic testing demonstrated that both activity and selectivity were strongly influenced by the support composition and morphology, with the 2D Mo–W composite outperforming MoS2 and WS2. All catalysts predominantly promoted selective CO hydrogenation to COL, while HCAL and HCOL remained minor products. The best performance was achieved with Pt supported on the 2D Mo–W–S composite prepared by microwave-assisted synthesis, delivering 75% CAL conversion with a COL selectivity and yield of 64% and 48%, respectively, achieved within 6 h.
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