A systematic study on the synthesis of a series of self-assembled suprastructures, such as cubes, stars, belts, and microspheres, of Ag nanoparticles (AgNPs) in borosilicate glassware heavily cleaned with aqua regia is presented. These self-assembled structures are mostly formed from the crystallographically iso-oriented AgNPs, and exhibit well-defined shapes. In regular washed glassware, only Ag nanowires are synthesized. The formation mechanisms of these self-assembled Ag structures, based on monitoring of their structural evolution in glassware decorated with different molecules, are proposed. This work not only demonstrates that the surface energy of glassware can affect chemical synthesis, but also provides an interesting approach to the shape-controlled synthesis of novel self-assembled suprastructures of AgNPs, which could be potentially used as synthesis templates, drug vessels, and microreactors.
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http://dx.doi.org/10.1002/smll.201001084 | DOI Listing |
Nanoscale Adv
June 2024
Department of Molecular Sciences, Swedish University of Agricultural Sciences Box 7015, 5, Almas allé Uppsala 75007 Sweden
Spherical particles with tunable anisotropic structures enabled by multiple surface functionalities have garnered interest for their potential applications in adsorption technologies. The presence of diverse functional groups in the surface layer, exhibiting varying acidity and hydrophilicity, can lead to unique characteristics in terms of surface structure and behaviour. In this study, the particles were synthesised using a two-step approach involving surface functionalisation of previously synthesised SiO Stöber particles.
View Article and Find Full Text PDFPhys Chem Chem Phys
June 2022
Sorbonne Université Department of Chemistry, 4 Place Jussieu, 75005 Paris, France.
Herein, we use a water-dispersive 3D suprastructure of ferrite (FeO) nanocrystals called supraballs. They are solid spherical assemblies of hydrophobic nanocrystals with a rather low Young's modulus compared to similar 3D superlattices deposited on a substrate. Using atomic force microscopy methods, their nanomechanical properties are measured, which show small flexibility and deformation.
View Article and Find Full Text PDFLangmuir
October 2021
Departamento de Fisica de Aplicada, Facultade de Fisica, Universidade de Santiago de Compostela, E-15782 Santiago de Compostela, Spain.
Chem Sci
December 2020
Laboratory of Supramolecular and Bio-Nanomaterials (SupraBioNanoLab), Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano Via Luigi Mancinelli 7 20131 Milan Italy
Nanoparticle (NP) self-assembly has led to the fabrication of an array of functional nanoscale systems, having diverse architectures and functionalities. In this perspective, we discuss the design and application of NP suprastructures (SPs) characterized by nanoconfined compartments in their self-assembled framework, providing an overview about SP synthetic strategies reported to date and the role of their confined nanocavities in applications in several high-end fields. We also set to give our contribution towards the formation of more advanced nanocompartmentalized SPs able to work in dynamic manners, discussing the opportunities of further advances in NP self-assembly and SP research.
View Article and Find Full Text PDFACS Nano
June 2021
State Key Laboratory of Heavy Oil Processing and School of Materials Science and Engineering, China University of Petroleum (East China), 66 Changjiang West Road, Qingdao 266580, China.
Helical supramolecular architectures play important structural and functional roles in biological systems. Although their occurrence is widely perceived to correlate to fundamental chiral units including l-amino acids and d-sugars, the detailed relationship between molecular and supramolecular handedness is still unclear. At the same time, although achiral units are practically always in close proximity to chiral ones by covalent linkage along a polymeric chain, their effect on supramolecular handedness has received relatively less attention.
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