Pd nanoparticles were successfully encapsulated inside mesoporous silicalite-1 nanocrystals (Pd@mnc-S1) by a one-pot method. The as-synthesized Pd@mnc-S1 with excellent stability functioned as an active and reusable heterogeneous catalyst. The unique porosity and nanostructure of silicalite-1 crystals endowed the Pd@mnc-S1 material general shape-selectivity for various catalytic reactions, including selective hydrogenation, oxidation, and carbon-carbon coupling reactions.

Superhydrophobic and superhydrophilic surfaces are of great interest because of a large range of applications, for example, as antifogging and self-cleaning coatings, as antibiofouling paints for boats, in metal refining, and for water-oil separation. An aqueous ink based on three-dimensional graphene monoliths (Gr) can be used for constructing both superhydrophobic and superhydrophilic surfaces on arbitrary substrates with different surficial structures from the meso- to the macroscale. The surface wettability of a Gr-coated surface mainly depends on which additional layers (air for a superhydrophobic surface and water for a superhydrophilic surface) are adsorbed on the surface of the graphene sheets. Switching a Gr-coated surface between being superhydrophobic and superhydrophilic can thus be easily achieved by drying and prewetting with ethanol. The Gr-based superhydrophobic membranes or films should have great potential as efficient separators for fast and gravity-driven oil-water separation.

The Kirkendall effect was utilized to synthesize mesoporous silicalite-1 zeolite nanocrystals without the involvement of additional templates. The mesopore size as well as the particle size can be easily controlled by nanoscale Kirkendall growth via significantly reducing the amount of water or tetrapropylammonium hydroxide, which were used in large quantities in conventional methods. The Kirkendall growth method is thus suitable for large-scale synthesis of mesoporous MFI zeolites with very high yields but low cost for practical applications.

Pd nanoparticles were successfully encapsulated inside mesoporous silicalite‐1 nanocrystals (Pd@mnc‐S1) by a one‐pot method. The as‐synthesized Pd@mnc‐S1 with excellent stability functioned as an active and reusable heterogeneous catalyst. The unique porosity and nanostructure of silicalite‐1 crystals endowed the Pd@mnc‐S1 material general shape‐selectivity for various catalytic reactions, including selective hydrogenation, oxidation, and carbon–carbon coupling reactions.

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