Surfactant-free assembling of functionalized single-walled carbon nanotube buckypapers

被引:37
|
作者
Anson-Casaos, A. [1 ]
Gonzalez-Dominguez, J. M. [1 ]
Terrado, E. [1 ]
Martinez, M. T. [1 ]
机构
[1] CSIC, Inst Carboquim, Zaragoza 50018, Spain
关键词
SIDEWALL FUNCTIONALIZATION; COMPOSITE FIBERS; FILMS; TRANSPARENT; PURIFICATION; SPECTROSCOPY; CHEMISTRY; POLYMER;
D O I
10.1016/j.carbon.2009.12.043
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
The electrical and textural properties of single-walled carbon nanotube buckypapers were tunned through chemical functionalizaton processes Single-walled carbon nanotubes (SWCNTs) were covalently functionalized with three different chemical groups Carboxylic acids (-COOH), benzylamine (-Ph-CH(2)-NH(2)), and perfluorooctylaniline (-Ph-(CF(2))(7)-CF(3)) Functionalized SWCNTs were dispersed in water or dimethylformamide (DMF) by sonication treatments without the addition of surfactants or polymers Carbon nanotube sheets (buckypapers) were prepared by vacuum filtration of the functionalized SWCNT dispersions The electrical conductivity, textural properties, and processability of the functionalized buckypapers were studied in terms of SWCNT purity, functionalization, and assembling conditions Carboxylated buckypapers demonstrated very low specific surface areas (< 1 m(2)/g) and roughness factor (R(a) = 14 nm), while aminated and fluorinated buckypapers exhibited roughness factors of around 70 nm and specific surface areas of 160180 m(2)/g Electrical conductivity for carboxylated buckypapers was higher than for as-grown SWCNTs, but for aminated and fluorinated SWCNTs it was lower than for as-grown SWCNTs This could be interpreted as a chemical inhibition of metallic SWCNTs due to the specificity of the diazonium salts reaction used to prepare the aminated and fluorinated SWCNTs The utilization of high purity as-grown SWCNTs positively influenced the mechanical characteristics and the electrical conductivity of functionalized buckypapers (C) 2009 Elsevier Ltd All rights reserved.
引用
收藏
页码:1480 / 1488
页数:9
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