Ref HAL: hal-02511718_v1
DOI: 10.1039/c9nr05710b
WoS: 000503282100021
Exporter : BibTex | endNote
2 Citations
Résumé:

Nano-porous two-dimensional molecular crystals, self-assembled on atomically flat host surfaces offer abroad range of possible applications, from molecular electronics to future nano-machines. Computerassisteddesigning of such complex structures requires numerically intensive modeling methods. Here wepresent the results of extensive, fully atomistic simulations of self-assembled monolayers of interdigitatedmolecules of 1,3,5-tristyrilbenzene substituted by C6 alkoxy peripheral chains (TSB3,5-C6), depositedonto highly-ordered pyrolytic graphite. Structural and electronic properties of the TSB3,5-C6 moleculeswere determined from ab initio calculations, then used in Molecular Dynamics simulations to analyze themechanism of formation, epitaxy, and stability of the TSB3,5-C6 nanoporous superlattice. We show thatthe monolayer disordering results from the competition between flexibility of the C6 chains and theirstabilization by interdigitation. The inclusion of guest molecules (benzene and pyrene) into superlatticenanopores stabilizes the monolayer. The alkoxy chain mobility and available pore space defines thesystems dynamics, essential for potential application.