Synthesis of covalently attached hexadecaanilines on carbon nanotubes: toward electronic nanocarbon preparation

被引:4
作者
Chiang, Long Y. [1 ]
Anandakathir, Robinson [1 ]
Hauck, Tanya S. [2 ]
Lee, Lawrence [2 ]
Canteenwala, Taizoon [1 ]
Padmawar, Prashant A. [1 ]
Pritzker, Kenneth [2 ]
Bruno, Ferdinando F. [3 ]
Samuelson, Lynne A. [3 ]
机构
[1] Univ Massachusetts, Dept Chem, Lowell, MA 01854 USA
[2] Univ Toronto, Pathol & Lab Med, Toronto, ON, Canada
[3] USA, RDECOM, Natick Soldier Ctr, Natick, MA 01760 USA
关键词
ELECTROCHEMICAL REDUCTION; DIAZONIUM SALTS; POLYANILINE; COMPOSITE; PERFORMANCE; FUNCTIONALIZATION; SUPERCAPACITORS; POLYMERIZATION; CAPACITANCE; SURFACES;
D O I
10.1039/b9nr00255c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe the direct covalent-grafting synthesis of well-defined aniline oligomers, such as tetraaniline (A(4)) and hexadecaaniline (A(16), major)/eicosaaniline (A(20), minor), on the sidewalls of carbon nanotubes (CNTs), via dediazonization reaction, for achieving highly soluble nanomaterials suitable for printing purposes, with long-term physical stability. Chemically grafting a layer of electroactive hexadecaanilines on CNTs resembles semiconductive encapsulation of functionalized CNTs. The resulting covalent nanoconjugates SWNT-(A(4))(x), MWNT-(A(4))(x), SWNT-(A(16/20))(x), and MWNT-(A(16/20))(x) were characterized by various spectroscopic and microscopic mapping methods. The combination of transmission electron microscopy (TEM) and electron energy loss spectroscopy (EELS) analyses provided direct evidence for A(16/20) attachment to the CNTs, giving confirmation of the presence of heteroatoms surrounding the CNTs that was absent in the parent CNTs. Subsequent atom mapping in the vicinity of the tube structure allowed us to illustrate the 3D distribution of heteroatoms along the CNT surface.
引用
收藏
页码:535 / 541
页数:7
相关论文
共 49 条
[1]   Covalent modification of carbon surfaces by aryl radicals generated from the electrochemical reduction of diazonium salts [J].
Allongue, P ;
Delamar, M ;
Desbat, B ;
Fagebaume, O ;
Hitmi, R ;
Pinson, J ;
Saveant, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (01) :201-207
[2]  
ANANTHARAJ V, 1999, CHEM SOC PERKIN T, V1, P3357
[3]   Functionalization of carbon nanotubes by electrochemical reduction of aryl diazonium salts: A bucky paper electrode [J].
Bahr, JL ;
Yang, JP ;
Kosynkin, DV ;
Bronikowski, MJ ;
Smalley, RE ;
Tour, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (27) :6536-6542
[4]   Highly functionalized carbon nanotubes using in situ generated diazonium compounds [J].
Bahr, JL ;
Tour, JM .
CHEMISTRY OF MATERIALS, 2001, 13 (11) :3823-+
[5]   Polyaniline and carbon nanotubes based composites containing whole units and fragments of nanotubes [J].
Baibarac, M ;
Baltog, I ;
Lefrant, S ;
Mevellec, JY ;
Chauvet, O .
CHEMISTRY OF MATERIALS, 2003, 15 (21) :4149-4156
[6]   Progress in preparation, processing and applications of polyaniline [J].
Bhadra, Sambhu ;
Khastgir, Dipak ;
Singha, Nikhil K. ;
Lee, Joong Hee .
PROGRESS IN POLYMER SCIENCE, 2009, 34 (08) :783-810
[7]   Synthesis of elastic core-shell conductive submicron to nanoparticles of penta(oligoanilinated) C60 [J].
Canteenwala, T ;
Patil, S ;
Halder, M ;
Chiang, LY .
SYNTHETIC METALS, 2003, 135 (1-3) :795-797
[8]   Electrochemical and capacitive properties of polyaniline-implanted porous carbon electrode for supercapacitors [J].
Chen, WC ;
Wen, TC .
JOURNAL OF POWER SOURCES, 2003, 117 (1-2) :273-282
[9]   Synthesis of a new polyaniline/nanotube composite:: "in-situ" polymerisation and charge transfer through site-selective interaction [J].
Cochet, M ;
Maser, WK ;
Benito, AM ;
Callejas, MA ;
Martínez, MT ;
Benoit, JM ;
Schreiber, J ;
Chauvet, O .
CHEMICAL COMMUNICATIONS, 2001, (16) :1450-1451
[10]   Physical doping of a conjugated polymer with carbon nanotubes [J].
Coleman, JN ;
Curran, S ;
Dalton, AB ;
Davey, AP ;
Mc Carthy, B ;
Blau, W ;
Barklie, RC .
SYNTHETIC METALS, 1999, 102 (1-3) :1174-1175