Publication

Tunable surface nanostructures from Block copolymer self-assembly

Abstract

Nanostructures are known to exhibit novel optical, electrical, and magnetic and many other interesting physical properties and a lot of research has been invested on the synthesis and study of such structures in the recent years. The massive drive towards miniaturization of devices heavily relies on the successful functioning of nanostructures. Self-assembly (or the bottom-up approaches) is emerging as an attractive tool for creating functional nanostructures owing to its simplicity and relatively low cost approaches. Nanostructures with high density and periodicity on surface are important in applications like high density data storage, sensors, catalyst support surfaces and other functional interfaces. Reverse micelles formed by the self-organization of amphiphilic diblock copolymer molecules have been used to create an array of polymer nanoparticles on silicon surface by spin coating . The formation of reverse micelles, the means of tuning their sizes and systematically varying the periodicities using solvent quality, solution concentration, deposition conditions and polymer molecular weight as handles will be presented. The hydrophilic core of the reverse micelles is capable of binding metal ions and so, inorganic nanoparticle arrays can be derived from these micelle arrays. The size of the nanoparticles in the array is further tunable by working on the loading conditions. The tunability of nanoparticle sizes will be presented as well.

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Related concepts (32)
Micelle
A micelle (maɪˈsɛl) or micella (maɪˈsɛlə) (plural micelles or micellae, respectively) is an aggregate (or supramolecular assembly) of surfactant amphipathic lipid molecules dispersed in a liquid, forming a colloidal suspension (also known as associated colloidal system). A typical micelle in water forms an aggregate with the hydrophilic "head" regions in contact with surrounding solvent, sequestering the hydrophobic single-tail regions in the micelle centre. This phase is caused by the packing behavior of single-tail lipids in a bilayer.
Self-assembly of nanoparticles
Nanoparticles are classified as having at least one of three dimensions be in the range of 1-100 nm. The small size of nanoparticles allows them to have unique characteristics which may not be possible on the macro-scale. Self-assembly is the spontaneous organization of smaller subunits to form larger, well-organized patterns. For nanoparticles, this spontaneous assembly is a consequence of interactions between the particles aimed at achieving a thermodynamic equilibrium and reducing the system’s free energy.
Self-assembly
Self-assembly is a process in which a disordered system of pre-existing components forms an organized structure or pattern as a consequence of specific, local interactions among the components themselves, without external direction. When the constitutive components are molecules, the process is termed molecular self-assembly. Self-assembly can be classified as either static or dynamic. In static self-assembly, the ordered state forms as a system approaches equilibrium, reducing its free energy.
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