ScholarWorks@성균관대학교

초록

Synergetic metal nanoparticles (NPs) and single atoms hold significant potential in reactions that require activating multiple substrate molecules. However, due to the differences in adsorption, activation and kinetics among distinct substrates during the multistep reaction process, the synergy and matching relationship between metal NPs and single atoms remain unclear. In this work, we synthesized a series of Co1-NP/CNT@CN-X dual-site catalysts with tunable molar ratios (X%) of Co single atoms to total Co species through a coordination site regulation (CSR) strategy and investigated the bucket effect of the dual active sites in the transfer hydrogenation of nitro compounds. Density functional theory calculations reveal that active hydrogen generation from ammonia borane hydrolysis primarily occurs at the surface of Co NPs, while nitroarenes hydrogenation predominantly takes place at Co single atoms, which is consistent with experimental findings. The optimized Co1-NP/CNT@CN-7.6 maintains high selectivity for nitro hydrogenation (> 99.9 %) and exhibits conversion (99.9 %) nearly 3.7 times that of the original Co1-NP/CNT@CN-1.6 catalyst (27 %), achieved by overcoming the bucket effect between Co NPs and single atoms. This work not only elucidates the synergistic mechanisms of dual sites in transfer hydrogenation, but also establishes that optimizing matching effect is an effective approach to significantly enhance their catalytic performance. © 2024 Elsevier B.V.

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