Zhong Yicheng, Mao Yuelin, Shi Shunli, Wan Mingming, Ma Chong, Wang Shuhua, Chen Chao, Zhao Dan, Zhang Ning
Key Laboratory of Jiangxi Province for Environment and Energy, College of Chemistry , Nanchang University , Nanchang , Jiangxi 330031 , P. R. China.
ACS Appl Mater Interfaces. 2019 Sep 4;11(35):32251-32260. doi: 10.1021/acsami.9b07864. Epub 2019 Aug 22.
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 FeO@Pd/ZIF-8@ZIF-8, possesses diverse functional structural features. The hollow cavity can improve mass transfer; superparamagnetic FeO 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 FeO@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.
通过将金属纳米颗粒(NPs)封装到金属有机框架(MOFs)中获得的MNPs@MOF催化剂在多相催化中表现出迷人的性能。长期以来,提高MNPs@MOF催化剂的催化活性和可重复使用性一直是一个巨大的挑战。在此,我们展示了精心设计的具有中空双壳结构和磁性的Pd/MOFs,其在氢化反应中表现出高可重复使用性、高效催化活性和尺寸选择性。合成的Pd/MOF,记为Void FeO@Pd/ZIF-8@ZIF-8,具有多种功能结构特征。中空腔可以改善传质;嵌入内MOF壳层的超顺磁性FeO NPs可以增强分离和可回收性;Pd NPs高度分散在内MOF壳层的基质中,外MOF壳层起到保护作用,防止Pd NPs浸出,并作为筛子实现尺寸选择性。作为概念验证,Void FeO@Pd/ZIF-8@ZIF-8催化剂在室温下对苯乙烯氢化表现出优异的性能。对于较高转化率(>90%),20次循环后活性仅降低10%,连续20次循环后较低转化率仅降低3.6%(从32.5%降至28.9%),表明该催化剂具有良好的固有可重复使用性。本文提出的结构提供了一种有效提高MNPs@MOF催化剂可重复使用性的策略,这将增加它们的实际应用。