Defective Metal‐Organic Frameworks with Tunable Porosity and Metal Active Sites for Significantly Improved Performance in Styrene Oxidation

Abstract

Metal active sites and sufficient porosity in metal-organic frameworks (MOFs) are crucial parameters determining the performances of catalysis, guest molecule adsorption, etc. Herein, through in situ introduction of Ru sites with different levels to Cu-BTC structure together with post-synthetic activation at 180 °C, a series of hierarchically porous CuRu-BTC (HP-CuRu-BTC) MOFs were obtained. Besides, selective thermal decomposition (STD) treatment was carried out at 240 °C to further tune the hierarchical pores and metal sites, yielding rare case of metal nanoparticles (NPs)@HP-CuRu-BTC composites. After full characterization by XRD, N2 physisorption, SEM, ICP and XPS, these HP-CuRu-BTC and NPs@HP-CuRu-BTC samples possess high surface area (682-1199 m2 g-1 ), hierarchical pores and highly distributed metal sites with reduced oxidation states (Cu+ and Ru2+ ), indicating regulation of both metal sites and hierarchical pores. The HP-CuRu-BTC and NPs@HP-CuRu-BTC were further employed as catalysts for the heterogeneous styrene oxidation reaction under mild condition. Compared to microporous Cu-BTC with unary metal component, HP-CuRu-BTC-3 and NPs@HP-CuRu-BTC-3 exhibited more than 2 times higher styrene conversion after 7 hours reaction under same condition.