Formation and Control of Porous Two-Dimensional Molecular Self-Assembly at Solid-Liquid Interfaces

2012 ◽  
Vol 70 (12) ◽  
pp. 1255-1266 ◽  
Author(s):  
Yoshito Tobe
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.


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

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).


2020 ◽  
pp. 1905784
Author(s):  
Shuai Zhang ◽  
Jiajun Chen ◽  
Jianli Liu ◽  
Harley Pyles ◽  
David Baker ◽  
...  

Langmuir ◽  
2002 ◽  
Vol 18 (21) ◽  
pp. 8085-8095 ◽  
Author(s):  
Orlando J. Rojas ◽  
Lubica Macakova ◽  
Eva Blomberg ◽  
Åsa Emmer ◽  
Per M. Claesson

2009 ◽  
Vol 08 (01n02) ◽  
pp. 119-122
Author(s):  
LI ZHANG ◽  
HUA-YAN SI ◽  
HUA XU ◽  
HAO-LI ZHANG ◽  
YU-QING XIONG

Highly ordered arrays consisting uniform fluorescent cadmium selenide ( CdSe ) quantum dots (QDs) ring or dot structures were obtained by self-assembly of QDs on chemically patterned substrates. In this method, Au substrates with alternating hydrophobic and hydrophilic square patterns are firstly fabricated by microcontact printing, which allows water droplets to condense on the hydrophilic regions to provide two-dimensional template arrays. The CdSe QDs are then assembled at the liquid/liquid interfaces to give uniform micro or nanostructures. The shape and size of the rings and dots can be tailored by controlling the relative evaporation speed of the water and the organic solvents. The obtained nanostructures have ideal topography to avoid substrate-induced fluorescence quenching.


Soft Matter ◽  
2014 ◽  
Vol 10 (15) ◽  
pp. 2612 ◽  
Author(s):  
Jinhua Cai ◽  
Haihui Chen ◽  
Jiangen Huang ◽  
Jingxia Wang ◽  
Dongliang Tian ◽  
...  

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