Polymers encapsulated in short single wall carbon nanotubes: Pseudo-1D morphologies and induced chirality

被引:11
|
作者
Kumar, Sunil [1 ]
Pattanayek, Sudip K. [1 ]
Pereira, Gerald G. [2 ]
机构
[1] Indian Inst Technol, Dept Chem Engn, New Delhi 110016, India
[2] CSIRO Math Informat & Stat, Clayton 3169, Australia
关键词
MOLECULAR-DYNAMICS SIMULATIONS; MECHANICAL-PROPERTIES; MONTE-CARLO; POLYETHYLENE; DNA; CHAIN; CRYSTALLIZATION; COMPOSITES; INSERTION; RADIUS;
D O I
10.1063/1.4914463
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Molecular dynamics simulations are performed to investigate the stable morphologies of semi-flexible polymer chains within a single wall carbon nanotube (CNT). We characterize these morphologies with a variety of measures. Due to the different curvature inside the CNT to outside, there are increased numbers of polymer-CNT bead contacts for polymers which reside inside the CNT. A sufficiently long polymer chain first adsorbs on the exterior of the nanotube and subsequently moves inside the cavity of the nanotube. At equilibrium, the polymer configuration consists of a central stem surrounded by helically wrapped layers. Sections of the polymer outside the CNT have helical conformations (for CNTs of small radius) or circular arrangements (for CNTs of larger radius). Polymers encapsulated within the CNT have an increased chirality due to packing of the beads and this chirality is further enhanced for moderately stiff chains. (C) 2015 AIP Publishing LLC.
引用
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页数:12
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