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.