Control of Fullerene Crystallization from 2D to 3D through Combined Solvent and Template Effects
Author(s) -
Daling Cui,
Maryam Ebrahimi,
Federico Rosei,
Jennifer MacLeod
Publication year - 2017
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.7b08642
Subject(s) - chemistry , solvent , molecule , crystallization , fullerene , nanoscopic scale , covalent bond , scanning tunneling microscope , chemical physics , density functional theory , adsorption , self assembly , nanotechnology , computational chemistry , organic chemistry , materials science
Achieving precise control of molecular self-assembly to form designed three-dimensional (3D) structures is a major goal in nanoscale science and technology. Using scanning tunnelling microscopy and density functional theory calculations, we show that a 2D covalent organic framework (COF-1) can template solution-processed C 60 guest molecules to form several solvent-dependent structural arrangements and morphologies via a 2D to 3D growth process. When 1,2,4-tricholorobenzene is used as solvent, C 60 molecules form a template-defined close-packed structure. When heptanoic acid is used as solvent, a range of lower density architectures that deviate from the template-defined close packing are observed. We attribute this difference to the co-adsorption of the heptanoic acid solvent molecules, which is only achieved in the presence of the template. This work demonstrates the possibility to precisely control 3D molecular self-assembly through the synergistic combination of template and solvent effects.
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