Nanotube functionalization and polymer grafting: An ab initio study

被引:68
|
作者
Mylvaganam, K [1 ]
Zhang, LC [1 ]
机构
[1] Univ Sydney, Sch Aerosp Mech & Mecatron Engn, Sydney, NSW 2006, Australia
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2004年 / 108卷 / 39期
关键词
D O I
10.1021/jp048061x
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
Functionalization of carbon nanotubes (CNTs) is important to increase their solubility and reactivity. This paper investigates possible ways of functionalizing CNTs using the methoxy radical and the secondary butyl anion as initiators and their reactions with ethylene and epoxide, leading to polyethylene- and polyepoxide-grafted nanotubes, with the aid of the density functional theory. The nanotubes were modeled by nanotube segments with H atoms added to the dangling bonds of the perimeter carbons. The study predicts that both free-radical and anionic functionalization methods are energetically favorable; that the resulting CNT radical and the CNT anion can react with ethylene and epoxide, respectively; and that the resulting products have free electrons and negative charges on the carbon and oxygen atoms at the free ends of ethylene and epoxide, respectively. Hence, the in situ free-radical and anionic polymerizations can propagate to produce polymer-grafted CNT. The cationic functionalization of CNTs using BF3 as an initiator was found to be infeasible.
引用
收藏
页码:15009 / 15012
页数:4
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