MESOSCALE COMPUTER SIMULATIONS OF POLYMER-TETHERED ORGANIC/INORGANIC NANOCUBE SELF-ASSEMBLY
| Autor: | Elaine R. Chan, Sharon C. Glotzer, Lin C. Ho |
|---|---|
| Rok vydání: | 2009 |
| Předmět: |
chemistry.chemical_classification
Nanostructure Materials science General Physics and Astronomy Nanoparticle Statistical and Nonlinear Physics Nanotechnology Polymer Silsesquioxane Computer Science Applications chemistry.chemical_compound Computational Theory and Mathematics chemistry Copolymer Brownian dynamics Molecule Self-assembly Mathematical Physics |
| Zdroj: | International Journal of Modern Physics C. 20:1443-1456 |
| ISSN: | 1793-6586 0129-1831 |
| DOI: | 10.1142/s0129183109014503 |
| Popis: | A molecular simulation study of the mesoscale self-assembly of tethered nanoparticles having a cubic geometry is presented. Minimal models of the tethered nanocubes are developed to represent a polyhedral oligomeric silsesquioxane (POSS) molecule with polymeric substituents. The models incorporate some of the essential structural features and interaction specificity of POSS molecules, and facilitate access to the long length and timescales pertinent to the assembly process while foregoing atomistic detail. The types of self-assembled nanostructures formed by the tethered nanocubes in solution are explored via Brownian dynamics simulations using these minimal models. The influence of various parameters, including the conditions of the surrounding medium, the molecular weight and chemical composition of the tether functionalities, and the number of tethers on the nanocube, on the formation of specific structures is demonstrated. The role of cubic nanoparticle geometry on self-assembly is also assessed by comparing the types of structures formed by tethered nanocubes and by their flexible coil triblock copolymer and tethered nanosphere counterparts. Morphological phase diagrams are proposed to describe the behavior of the tethered nanocubes. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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