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表面活性剂胺对半导体单壁碳纳米管的富集机制

Enrichment mechanism of semiconducting single-walled carbon nanotubes by surfactant amines.

作者信息

Ju Sang-Yong, Utz Marcel, Papadimitrakopoulos Fotios

机构信息

Nanomaterials Optoelectronics Laboratory, Polymer Program, Institute of Materials Science, University of Connecticut, Storrs, Connecticut 06269, USA.

出版信息

J Am Chem Soc. 2009 May 20;131(19):6775-84. doi: 10.1021/ja809054c.

Abstract

Utilization of single-walled carbon nanotubes (SWNTs) in high-end applications hinges on separating metallic (met-) from semiconducting (sem-) SWNTs. Surfactant amines, like octadecylamine (ODA) have proven instrumental for the selective extraction of sem-SWNTs from tetrahydrofuran (THF) nanotube suspensions. The chemical shift differences along the tail of an asymmetric, diacetylenic surfactant amine were used to probe the molecular dynamics in the presence and absence of nanotubes via NMR. The results suggest that the surfactant amine head is firmly immobilized onto the nanotube surface together with acidic water, while the aliphatic tail progressively gains larger mobility as it gets farther from the SWNT. X-ray and high-resolution TEM studies indicate that the sem-enriched sample is populated mainly by small nanotube bundles containing ca. three SWNTs. Molecular simulations in conjunction with previously determined HNO(3)/H(2)SO(4) oxidation depths for met- and sem-SWNTs indicate that the strong pinning of the amine surfactants on the sem-enriched SWNTs bundles is a result of a well-ordered arrangement of nitrate/amine salts separated with a monomolecular layer of H(2)O. Such continuous 2D arrangement of nitrate/amine salts shields the local environment adjacent to sem-enriched SWNTs bundles and maintains an acidic pH that preserves nanotube oxidation (i.e., SWNT(n+)). This, in turn, results in strong interactions with charge-balancing NO(3)(-) counterions that through their association with neutralized surfactant amines provide effective THF dispersion and consequent sem enrichment.

摘要

单壁碳纳米管(SWNTs)在高端应用中的使用取决于从金属性(met-)单壁碳纳米管中分离出半导体性(sem-)单壁碳纳米管。表面活性剂胺,如十八烷基胺(ODA),已被证明有助于从四氢呋喃(THF)纳米管悬浮液中选择性提取半导体性单壁碳纳米管。通过核磁共振(NMR),利用不对称二乙炔基表面活性剂胺尾部的化学位移差异来探测有无纳米管时的分子动力学。结果表明,表面活性剂胺头部与酸性水一起牢固地固定在纳米管表面,而脂肪族尾部随着远离单壁碳纳米管,其流动性逐渐增大。X射线和高分辨率透射电子显微镜(TEM)研究表明,富含半导体性单壁碳纳米管的样品主要由包含约三根单壁碳纳米管的小纳米管束组成。结合先前确定的金属性和半导体性单壁碳纳米管的硝酸/硫酸氧化深度进行的分子模拟表明,胺表面活性剂在富含半导体性单壁碳纳米管束上的强烈固定是由硝酸/胺盐的有序排列导致的,这些盐被一层水分子隔开。这种硝酸/胺盐的连续二维排列屏蔽了富含半导体性单壁碳纳米管束附近的局部环境,并保持了酸性pH值,从而维持纳米管的氧化(即SWNT(n+))。反过来,这又导致与电荷平衡的硝酸根(NO3(-))反离子发生强烈相互作用,这些反离子通过与中和的表面活性剂胺缔合,提供了有效的四氢呋喃分散作用,从而实现了半导体性单壁碳纳米管的富集。

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