ANISOKINEQ
Equilibrium properties and kinetics of self-assembly of anisotropic colloids and molecular liquids
| Coordinatore | UNIVERSIDAD COMPLUTENSE DE MADRID
Organization address
address: AVENIDA DE SENECA 2 contact info |
| Nazionalità Coordinatore | Spain [ES] |
| Totale costo | 50˙000 € |
| EC contributo | 50˙000 € |
| Programma | FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
| Code Call | FP7-PEOPLE-2011-CIG |
| Funding Scheme | MC-CIG |
| Anno di inizio | 2012 |
| Periodo (anno-mese-giorno) | 2012-04-01 - 2014-03-31 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
UNIVERSIDAD COMPLUTENSE DE MADRID
Organization address
address: AVENIDA DE SENECA 2 contact info |
ES (MADRID) | coordinator | 50˙000.00 |
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Obiettivo del progetto (Objective)
'The proposed research project aims to study self-assembly of new materials made of anisotropic colloids as building blocks and to unravel the mechanism of crystallization in molecular liquids, such as water.
The last few decades have seen a huge growth in the research on novel soft materials to be exploited in nanotechnology, and an efficient route to build them is to make use of self-assembly. The term self-assembly refers to the reversible and cooperative assembly of predefined components into an ordered super- structure. Self-assembly is responsible for nanostructure formation in colloidal, amphiphilic, polymeric, and biomolecular materials. However, unlike most of the work of the last decade on particle self-assembly, which has focused on colloidal systems of spherically-shaped particles with isotropic interactions, not enough effort has been put yet into understanding and controlling the self-assembly mechanism in suspensions of irregularly shaped or/and anisotropically interacting colloidal particles (the latter also called 'patchy colloids'). Patchy colloids have been recently used to reproduce the colloidal analogue of a vitally important molecule: water. Water is the only known non-metallic substance that expands when freezing. Understanding the mechanism of water crystallisation (or ice formation) is of fundamental interest to many scientific disciplines, ranging from meteorology to food science and biology. However, on the one side length and time scale relevant for water crystallisation are unattainable with up-to-date experimental techniques. On the other side, computer simulations of ice crystallisation have been a great challenge, the difficulty been that hydrogen bonding between individual water molecules yields a disordered three-dimensional hydrogen-bond network that hinder ice formation. Therefore, understanding the mechanism of crystallisation of water still remains an open and challenging question.'