纳米材料基催化剂
材料科学
催化作用
可重用性
金属有机骨架
选择性
化学工程
介孔材料
纳米技术
纳米反应器
苯乙烯
纳米材料
纳米颗粒
超顺磁性
吸附
有机化学
共聚物
化学
聚合物
复合材料
磁化
工程类
计算机科学
软件
磁场
程序设计语言
物理
量子力学
作者
Yicheng Zhong,Yuelin Mao,Shunli Shi,Mingming Wan,Chong Ma,Shuhua Wang,Chao Chen,Dan Zhao,Ning Zhang
标识
DOI:10.1021/acsami.9b07864
摘要
MNPs@MOF catalysts obtained by encapsulating metal nanoparticles (NPs) into metal-organic frameworks (MOFs) show fascinating performance in heterogeneous catalysis. The improvement of catalytic activity and reusability of MNPs@MOF catalysts has been a great challenge for a long time. Herein, we demonstrate well-designed Pd/MOFs, featuring hollow double-shell structure and magnetic property, exhibiting high reusability, efficient catalytic activity, and size selectivity for hydrogenation reaction. The as-synthesized Pd/MOF, denoted as Void nFe3O4@Pd/ZIF-8@ZIF-8, possesses diverse functional structural features. The hollow cavity can improve mass transfer; superparamagnetic Fe3O4 NPs embedded in the inner MOF shell can enhance the separation and recyclability; Pd NPs are highly dispersed in the matrix of the inner MOF shell, and the outer MOF shell acts as a protector to prevent the leaching of Pd NPs and a sieve to achieve size selectivity. As a proof of concept, the Void nFe3O4@Pd/ZIF-8@ZIF-8 catalyst exhibited excellent performance for the hydrogenation of styrene at room temperature. The activity only reduced 10% after 20 cycles for the higher conversions (>90%), and the lower conversion only decreased 3.6% (from 32.5 to 28.9% conversion) after twenty consecutive cycles, indicating the good and intrinsic reusability of the catalyst. The proposed structure in this work provides a strategy to effectively improve the reusability of MNPs@MOF catalysts, which would increase their practical applications.
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