A Bottom-Up Approach to Solution-Processed, Atomically Precise Graphitic Cylinders on Graphite

被引:52
|
作者
Leonhardt, Erik J. [1 ]
Van Raden, Jeff M. [1 ]
Miller, David [2 ]
Zakharov, Lev N. [3 ]
Aleman, Benjamin [2 ]
Jasti, Ramesh [1 ]
机构
[1] Univ Oregon, Dept Chem & Biochem, Inst Mat Sci, Eugene, OR 97403 USA
[2] Univ Oregon, Ctr Opt Mol & Quantum Sci, Inst Mat Sci, Dept Phys, Eugene, OR 97403 USA
[3] Univ Oregon, CAMCOR Ctr Adv Mat Characterizat Oregon, Eugene, OR 97403 USA
基金
美国国家科学基金会;
关键词
Cycloparaphenylene; nanohoop; carbon nanotube; self-assembly; epitaxial growth; vertical alignment; CARBON NANOTUBES; GROWTH; CYCLOPARAPHENYLENES; TRANSPORT; STRATEGY; N=8-13; SPACE;
D O I
10.1021/acs.nanolett.8b03979
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Extended carbon nanostructures, such as carbon nanotubes (CNTs), exhibit remarkable properties but are difficult to synthesize uniformly. Herein, we present a new class of carbon nanomaterials constructed via the bottom up self-assembly of cylindrical, atomically precise small molecules. Guided by supramolecular design principles and circle packing theory, we have designed and synthesized a fluorinated nanohoop that, in the solid state, self-assembles into nanotube-like arrays with channel diameters of precisely 1.63 nm. A mild solution-casting technique is then used to construct vertical "forests" of these arrays on a highly ordered pyrolytic graphite (HOPG) surface through epitaxial growth. Furthermore, we show that a basic property of nanohoops, fluorescence, is readily transferred to the bulk phase, implying that the properties of these materials can be directly altered via precise functionalization of their nanohoop building blocks. The strategy presented is expected to have broader applications in the development of new graphitic nanomaterials with g-rich cavities reminiscent of CNTs.
引用
收藏
页码:7991 / 7997
页数:7
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