scholarly journals Directed self-assembly of inorganic nanoparticles at air/liquid interfaces

Nanoscale ◽  
2016 ◽  
Vol 8 (37) ◽  
pp. 16589-16595 ◽  
Author(s):  
Juan J. Giner-Casares ◽  
Javier Reguera
Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1502
Author(s):  
Johannes M. Parikka ◽  
Karolina Sokołowska ◽  
Nemanja Markešević ◽  
J. Jussi Toppari

The predictable nature of deoxyribonucleic acid (DNA) interactions enables assembly of DNA into almost any arbitrary shape with programmable features of nanometer precision. The recent progress of DNA nanotechnology has allowed production of an even wider gamut of possible shapes with high-yield and error-free assembly processes. Most of these structures are, however, limited in size to a nanometer scale. To overcome this limitation, a plethora of studies has been carried out to form larger structures using DNA assemblies as building blocks or tiles. Therefore, DNA tiles have become one of the most widely used building blocks for engineering large, intricate structures with nanometer precision. To create even larger assemblies with highly organized patterns, scientists have developed a variety of structural design principles and assembly methods. This review first summarizes currently available DNA tile toolboxes and the basic principles of lattice formation and hierarchical self-assembly using DNA tiles. Special emphasis is given to the forces involved in the assembly process in liquid-liquid and at solid-liquid interfaces, and how to master them to reach the optimum balance between the involved interactions for successful self-assembly. In addition, we focus on the recent approaches that have shown great potential for the controlled immobilization and positioning of DNA nanostructures on different surfaces. The ability to position DNA objects in a controllable manner on technologically relevant surfaces is one step forward towards the integration of DNA-based materials into nanoelectronic and sensor devices.


Author(s):  
Shriram Pillapakkam ◽  
N. A. Musunuri ◽  
P. Singh

In this paper, we present a technique for freezing monolayers of micron and sub-micron sized particles onto the surface of a flexible thin film after the self-assembly of a particle monolayer on fluid-liquid interfaces has been improved by the process we have developed where an electric field is applied in the direction normal to the interface. Particles smaller than about 10 microns do not self-assemble under the action of lateral capillary forces alone since capillary forces amongst them are small compared to Brownian forces. We have overcome this problem by applying an electric field in the direction normal to the interface which gives rise to dipoledipole and capillary forces which cause the particles to arrange in a triangular pattern. The technique involves assembling the monolayer on the interface between a UV-curable resin and another liquid by applying an electric field, and then curing the resin by applying UV light. The monolayer becomes embedded on the surface of the solidified resin film.


Author(s):  
E. Amah ◽  
N. Musunuri ◽  
Ian S. Fischer ◽  
Pushpendra Singh

We numerically study the process of self-assembly of particle mixtures on fluid-liquid interfaces when an electric field is applied in the direction normal to the interface. The force law for the dependence of the electric field induced dipole-dipole and capillary forces on the distance between the particles and their physical properties obtained in an earlier study by performing direct numerical simulations is used for conducting simulations. The inter-particle forces cause mixtures of nanoparticles to self-assemble into molecular-like hierarchical arrangements consisting of composite particles which are organized in a pattern. However, there is a critical electric intensity value below which particles move under the influence of Brownian forces and do not self-assemble. Above the critical value, when the particles sizes differed by a factor of two or more, the composite particle has a larger particle at its core and several smaller particles forming a ring around it. Approximately same sized particles, when their concentrations are approximately equal, form binary particles or chains (analogous to polymeric molecules) in which positively and negatively polarized particles alternate, but when their concentrations differ the particles whose concentration is larger form rings around the particles with smaller concentration.


Author(s):  
Uvinduni I. Premadasa ◽  
Ying-Zhong Ma ◽  
Robert L. Sacci ◽  
Vera Bocharova ◽  
Nikki A. Thiele ◽  
...  

2017 ◽  
Vol 8 (2) ◽  
pp. 1350-1355 ◽  
Author(s):  
Alexander S. Groombridge ◽  
Aniello Palma ◽  
Richard M. Parker ◽  
Chris Abell ◽  
Oren A. Scherman

The successful self-assembly of a stimuli-responsive aqueous supramolecular hyperbranched polymer from small molecules and the macrocyclic host cucurbit[8]uril (CB[8]) is reported. This self-healing supramolecular network can act as a soft matter barrier at liquid–liquid interfaces.


Langmuir ◽  
2016 ◽  
Vol 33 (1) ◽  
pp. 372-381 ◽  
Author(s):  
Roozbeh Hajiraissi ◽  
Ignacio Giner ◽  
Guido Grundmeier ◽  
Adrian Keller

Impact ◽  
2020 ◽  
Vol 2020 (1) ◽  
pp. 38-40
Author(s):  
Ayae Sugawara-Narutaki

Nature oversees a vast array of amazing shapes formed by organisms such as plants, fungi and animals. Some of these manifest as intricate patterns in structures like coral and the nests of insects and birds. Associate Professor Ayae Sugawara-Narutaki, from the Department of Materials Chemistry at Nagoya University, Japan has a particular interest in these patterns. Sugawara-Narutaki's team focuses on research inspired by these self-organised nanostructures to develop nanomaterials for a variety of health-related applications. The ability of these nanomaterials to self-assemble and self-organise in a liquid phase has attracted a great deal of interest from materials scientists the world over.


2017 ◽  
Vol 8 (2) ◽  
pp. 370-374 ◽  
Author(s):  
Yang Zheng ◽  
Yucheng Huang ◽  
Zaid M. Abbas ◽  
Brian C. Benicewicz

The first case of surface-initiated polymerization-induced self-assembly (SI-PISA) of inorganic nanoparticles (NPs) into single-walled vesicles is reported.


Nanoscale ◽  
2018 ◽  
Vol 10 (7) ◽  
pp. 3438-3443 ◽  
Author(s):  
Zhen-Feng Cai ◽  
Hui-Juan Yan ◽  
Dong Wang ◽  
Li-Jun Wan

We report the potential and concentration controlled assembly of an alkyl-substituted benzo[1,2-b:4,5-b′]dithiophene (DDBDT) on an Au(111) electrode byin situelectrochemical scanning tunneling microscopy (ECSTM).


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