Control of Fullerene Crystallization from 2D to 3D through Combined Solvent and Template Effects

被引:29
|
作者
Cui, Daling [1 ]
Ebrahimi, Maryam [1 ]
Rosei, Federico [1 ,2 ]
Macleod, Jennifer M. [1 ,3 ]
机构
[1] Inst Natl Rech Sci, Ctr Energie Mat & Telecommun, 1650 Blvd Lionel Boulet, Varennes, PQ J3X 1S2, Canada
[2] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Sichuan, Peoples R China
[3] Queensland Univ Technol, Sch Chem Phys & Mech Engn, Brisbane, Qld 4000, Australia
基金
加拿大自然科学与工程研究理事会; 澳大利亚研究理事会; 加拿大创新基金会;
关键词
LIQUID-SOLID INTERFACE; FILM GROWTH; SURFACE; CRYSTALS; POLYMORPHISM; C-60; NUCLEATION; ACID; STABILIZATION; ORGANIZATION;
D O I
10.1021/jacs.7b08642
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:16732 / 16740
页数:9
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