| Literature DB >> 31927906 |
Yangyang Zhu1, Wei David Wang1, Xun Sun2, Mengying Fan1, Xiwei Hu1, Zhengping Dong1.
Abstract
Metal-nanocluster-doped porous materials are attracting considerable research attention due to their specific catalytic performance. In this study, core-shell metal-organic frameworks@covalent organic polymer (MOF@COP) nanocomposites were formed by the covalent linking of chemically stable COP on the surface of size-selective UiO-66-NH2. Pd nanoclusters with an average diameter of ∼0.8 nm were successfully confined in UiO-66-NH2@COP, and the obtained nanoreactor, referred to as UiO-66-NH2@COP@Pd, exhibited abundant porosity, high stability, and large surface area. Notably, the UiO-66-NH2@COP@Pd nanoreactor exhibited superior catalytic activity and stability for the catalytic reduction of 4-nitrophenol and hydrogenation of other nitroarenes, demonstrating the potential of Pd-cluster-doped MOF@COP hybrid materials as candidates for efficient catalytic hydrogenation. This study may provide new avenues for the construction of MOF@COP-hybrid-material-based heterogeneous catalysts for efficient catalytic applications.Entities:
Keywords: Pd nanoclusters; catalytic hydrogenation; core−shell MOF@COP hybrid materials; covalent organic polymers; nanoreactor; nitroarenes
Year: 2020 PMID: 31927906 DOI: 10.1021/acsami.9b21802
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229