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Self-Assembled Open Porous Nanoparticle Superstructures. | LitMetric

Self-Assembled Open Porous Nanoparticle Superstructures.

J Am Chem Soc

Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, P. R. China.

Published: August 2021

AI Article Synopsis

  • Researchers are exploring how to create open porous structures in inorganic nanoparticle assemblies, which could enhance their properties and broaden their applications.
  • The study reveals a method for forming these structures by assembling nanoparticles within 1D nanotubes, leading to non-close-packed arrangements.
  • Adjusting the size ratios of the nanotubes to nanoparticles allows for different structural configurations, while blocking the nanotube interiors can change the assembly process, affecting porosity and catalytic efficiency.

Article Abstract

Imparting porosity to inorganic nanoparticle assemblies to build up self-assembled open porous nanoparticle superstructures represents one of the most challenging issues and will reshape the property and application scope of traditional inorganic nanoparticle solids. Herein, we discovered how to engineer open pores into diverse ordered nanoparticle superstructures via their inclusion-induced assembly within 1D nanotubes, akin to the molecular host-guest complexation. The open porous structure of self-assembled composites is generated from nonclose-packing of nanoparticles in 1D confined space. Tuning the size ratios of the tube-to-nanoparticle enables the structural modulation of these porous nanoparticle superstructures, with symmetries such as , zigzag, , , and . Moreover, when the internal surface of the nanotubes is blocked by molecular additives, the nanoparticles would switch their assembly pathway and self-assemble on the external surface of the nanotubes without the formation of porous nanoparticle assemblies. We also show that the open porous nanoparticle superstructures can be ideal candidate for catalysis with accelerated reaction rates.

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Source
http://dx.doi.org/10.1021/jacs.1c04784DOI Listing

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