摘要
Graphical Surface modification by FeO x is introduced to remarkably improve the selectivity of cinnamyl alcohol in cinnamaldehyde hydrogenation over Pt/H-MoO 3 . The abundant Pt–FeO x interface and acidic surface contribute to the remarkably improved selectivity and activity. Hydrogenation of α,β-unsaturated aldehydes to unsaturated alcohols suffers a huge challenge in chemoselectivity. Herein, surface decoration by FeO x is introduced to remarkably improve the selectivity of cinnamyl alcohol (COL) in cinnamaldehyde (CAL) hydrogenation on Pt/MoO 3−y . The enhanced acidity on Pt–FeO x interfaces is beneficial for the chemisorption and activation of C=O bonds, promoting selective hydrogenation. The optimal catalysts with defined FeO x decoration afford efficient and chemoselective CAL hydrogenation (91.3 % selectivity) under mild conditions ( P H2 =1 MPa, T= 30 °C). Moreover, such innovation is further extended to develop other efficient metal (Ir, Rh and Pd) catalysts, identifying a universal promotion to Pt-group metals. This work is anticipated to inspire the rational design of high-performance catalysts via effective surface/interface engineering.
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