Cai Mengke, Li Yinle, Liu Qinglin, Xue Ziqian, Wang Haiping, Fan Yanan, Zhu Kelong, Ke Zhuofeng, Su Cheng-Yong, Li Guangqin
MOE Laboratory of Bioinorganic and Synthetic Chemistry Lehn Institute of Functional Materials School of Chemistry Sun Yat-Sen University Guangzhou 510275 P. R. China.
Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Materials Science and Engineering Sun Yat-Sen University Guangzhou 510275 P. R. China.
Adv Sci (Weinh). 2019 Feb 20;6(8):1802365. doi: 10.1002/advs.201802365. eCollection 2019 Apr 17.
The exploration of novel porous core-shell materials is of great significance because of their prospectively improved performance and extensive applications in separation, energy conversion, and catalysis. Here, mesoporous metal-organic frameworks (MOFs) NH-MIL-101(Fe) as a core generate a shell with mesoporous covalent organic frameworks (COFs) NUT-COF-1(NTU) by a covalent linking process, the composite NH-MIL-101(Fe)@NTU keeping retentive crystallinity with hierarchical porosity well. Importantly, the NH-MIL-101(Fe)@NTU composite shows significantly enhanced catalytic conversion and selectivity during styrene oxidation. It is mainly due to the hydrophilic MOF nanocrystals readily gathering the hydrophobic reactants styrene and boosting the radical mechanism path after combining the hydrophobic COFs shell. The synthetic strategy in this systematic study develops a new rational design for the synthesis of other core-shell MOF/COF-based hybrid materials, which can expand the promising applications.
探索新型多孔核壳材料具有重要意义,因为它们有望提升性能,并在分离、能量转换和催化等领域有广泛应用。在此,介孔金属有机框架(MOF)NH-MIL-101(Fe)作为核心,通过共价连接过程生成了带有介孔共价有机框架(COF)NUT-COF-1(NTU)的壳层,复合结构NH-MIL-101(Fe)@NTU保持了良好的结晶度和分级孔隙率。重要的是,NH-MIL-101(Fe)@NTU复合材料在苯乙烯氧化过程中表现出显著增强的催化转化率和选择性。这主要是由于亲水性的MOF纳米晶体易于聚集疏水性反应物苯乙烯,并在结合疏水性COF壳层后促进了自由基反应机理路径。本系统研究中的合成策略为合成其他基于MOF/COF的核壳杂化材料开发了一种新的合理设计方法,这可以拓展其广阔的应用前景。