徐来副教授课题组与苏州大学材化部黄小青教授课题组合作在Journal of the American Chemical Society上发表论文



On-Demand, Ultraselective Hydrogenation System Enabled by Precisely Modulated Pd–Cd Nanocubes


Yonggang Feng‡1, Weiwei Xu‡2, Bolong Huang‡3,Qi Shao1, Lai Xu*2, Shize Yang4,and Xiaoqing Huang*1


1 College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Jiangsu 215123, China

2 Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Jiangsu 215123, China

3 Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR

4 Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, New York 11973, United States


The pursuit of efficient hydrogenation nanocatalysts with a desirable selectivity toward intricate substrates is state-of-the-art research but remains a formidable challenge. Herein, we report a series of novel PdCdx nanocubes (NCs) for ultraselective hydrogenation reactions with flexible tuning features. Obtaining a desirable conversion level of the substrates (e.g., 4-nitrophenylacetylene (NPA), 4-nitrobenzaldehyde (NBAD), and 4-nitrostyrene (NS)) and competitive selectivity for all potential hydrogenation products have been achieved one by one under optimized hydrogenation conditions. The performance of these PdCdx NCs displays an evident dependence on both the composition and the use of Cd and a need for a distinct hydrogen source (H2 or HCOONH4). Additionally, for the selectivity of hydrogen to be suitably high, the morphology of the NCs has a very well defined effect. Density functional theory calculations confirmed the variation of adsorption  energy for the substrate and hydrogenation products by carefully controlled introduction of Cd, leading to a desirable level of selectivity for all potential hydrogenation products. The PdCdx NCs also exhibit excellent reusability with negligible activity/selectivity decay and structural/composition changes after consecutive reactions. The present study provides an advanced strategy for the rational design of superior hydrogenation nanocatalysts to achieve a practical application for desirable and selective hydrogenation reaction efficiency.








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