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Fullerene-based one-dimensional crystalline nanopolymer formed through topochemical transformation of the parent nanowire
Journal article   Open access

Fullerene-based one-dimensional crystalline nanopolymer formed through topochemical transformation of the parent nanowire

Junfeng Geng, Ilia A. Solov'yov, David G. Reid, Paul Skelton, Andrew E. H. Wheatley, Andrey V. Solov'yov and Brian F. G. Johnson
Physical review. B, Condensed matter and materials physics, Vol.81(21), 214114
17/06/2010

Abstract

Materials Science Materials Science, Multidisciplinary Physical Sciences Physics Physics, Applied Physics, Condensed Matter Science & Technology Technology
Large-scale practical applications of fullerene (C(60)) in nanodevices could be significantly facilitated if the commercially available micrometer-scale raw C(60) powder were further processed into a one-dimensional nanowire-related polymer displaying covalent bonding as molecular interlinks and resembling traditional important conjugated polymers. However, there has been little study thus far in this area despite the abundant literature on fullerene. Here we report the preparation and characterization of such a C(60)-based polymer nanowire, (-C(60)TMB-)(n), where TMB=1,2,4-trimethylbenzene, which displays a well-defined crystalline nanostructure, exceptionally large length-to-width ratio and excellent thermal stability. The material is prepared by first growing the corresponding nanowire through a solution phase of C(60) followed by a topochemical polymerization reaction in the solid state. Gas chromatography, mass spectrometry and (13)C nuclear magnetic resonance evidence is provided for the nature of the covalent bonding mode adopted by the polymeric chains. Theoretical analysis based on detailed calculations of the reaction energetics and structural analysis provides an in-depth understanding of the polymerization pathway. The nanopolymer promises important applications in biological fields and in the development of optical, electrical, and magnetic nanodevices.
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https://arxiv.org/pdf/0906.2216View
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