Immobilizing Metal Nanoparticles on Hierarchically Porous Organic Cages with Size Control for Enhanced Catalysis

Incorporating metal nanoparticles (MNPs) into porous composites with controlled size and spatial distributions is beneficial for a broad range of applications, but it remains a synthetic challenge. Here, we present a method to immobilize a series of highly dispersed MNPs (Pd, Ir, Pt, Rh, and Ru) with controlled size (<2 nm) on hierarchically micro-and mesoporous organic cage supports. Specifically, the metal-ionic surfactant complexes serve as both metal precursors and mesopore-forming agents during self-assembly with a microporous imine cage CC3, resulting in a uniform distribution of metal precursors across the resultant supports. The functional heads on the ionic surfactants as binding sites, together with the nanoconfinement of pores, guide the nucleation and growth of MNPs and prevent their agglomeration after chemical reduction. Moreover, the as-synthesized Pd NPs exhibit remarkable activity and selectivity in the tandem reaction due to the advantages of ultrasmall particle size and improved mass diffusion facilitated by the hierarchical pores.

Automated summary

Incorporating metal nanoparticles (MNPs) with controlled size and spatial distributions into porous composites is challenging but beneficial for various applications. This study presents a method to immobilize highly dispersed MNPs (Pd, Ir, Pt, Rh, and Ru) with controlled size (<2 nm) on hierarchically micro-and mesoporous organic cage supports. The functional heads on the ionic surfactants and nanoconfinement of pores guide the nucleation and growth of MNPs, resulting in a uniform distribution and prevention of agglomeration.