4.7 Article

Sheet-like silicalite-1 single crystals with embedded macropores displaying superior catalytic performance

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INORGANIC CHEMISTRY FRONTIERS
卷 10, 期 23, 页码 6998-7009

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d3qi01712e

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A unique method using urea-assisted dry-gel synthesis was employed to prepare sheet-like Silicalite-1 single crystals with intracrystalline macropores (HMS-Silicalite-1). These crystals exhibited enhanced catalytic performance compared to conventional Silicalite-1 and hierarchical macro/microporous Silicalite-1, making them highly efficient catalysts for diffusion-limited reactions.
Unique sheet-like Silicalite-1 single crystals containing intracrystalline macropores (HMS-Silicalite-1) were prepared by urea-assisted, dry-gel synthesis, which uses mesoporous silica spheres (MSSs) as both the silica precursor and the macropore template. Urea was found to inhibit crystal growth in the b-axis direction and, therefore, play a pivotal role in the formation of the sheet-like crystals. Zeolite growth occurred via dissolution-crystallization transformation of MSSs to produce macro/microporous Silicalite-1 crystals. Systematic studies revealed that the urea/SiO2 and H2O/SiO2 ratios affect the morphology of the resulting Silicalite-1 zeolites and that the thickness of HMS-Silicalite-1 platelets can be tuned between 190 nm and 400 nm. It was also found that the H2O/SiO2 and urea/SiO2 ratios can be modulated to match the inhibition and dissolution-crystallization processes. HMS-Silicalite-1 was assessed as a catalyst for the Beckmann rearrangement of cyclohexanone oxime to epsilon-caprolactam and found to exhibit significantly greater resistance to deactivation than conventional Silicalite-1 and hierarchical macro/microporous Silicalite-1. The superior performance of HMS-Silicalite-1 is attributed to the presence of crystals of Silicalite-1 that are thin in the direction of the b-axis and contain significant macropores (150 to 400 nm in size). The results of this study offer a novel, yet simple, method for simultaneous control of the zeolite crystal aspect ratio and macropore content to produce catalysts that are highly efficient for diffusion-limited reactions involving large reactant molecules.

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