Scalable Functional Group Engineering of Carbon Nanotubes by Improved One-Step Nitrene Chemistry

被引:141
作者
Gao, Chao [1 ,2 ]
He, Hongkun [3 ]
Zhou, Li [1 ,2 ]
Zheng, Xing [3 ]
Zhang, Yu [3 ]
机构
[1] Zhejiang Univ, Minist Educ, Dept Polymer Sci & Engn, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ, Minist Educ, Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Peoples R China
[3] Shanghai Jiao Tong Univ, Coll Chem & Chem Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSFER RADICAL POLYMERIZATION; RING-OPENING POLYMERIZATION; TRIPLET ALKYL NITRENES; ALPHA-AZIDOACETOPHENONES; 2+1 CYCLOADDITION; SURFACE; PHOTOLYSIS; SIDEWALL; BRUSHES; NANOCOMPOSITES;
D O I
10.1021/cm802704c
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
A facile, green, low cost and efficient one-step technology to synthesize highly dispersible functional single-walled and multiwalled carbon nanotubes (f-SWNTs and f-MWNTs) up to supergrams is reported. Large-scale (up to hundreds of grams) synthesis of functional azides was developed at first, and various reactive groups (i.e., -OH, -NH2, -COOH, and -Br) were then introduced onto the convex surfaces of CNTs in merely one reaction of nitrene addition under a relatively mild condition without causing significant damage to nanotubes. The contents of the functional moieties can be easily controlled by adjusting the feed ratio of the azide compounds to CNTs. In order to demonstrate the reactivity and functions of the immobilized organic moieties, different chemical reactions, including surface-initiated polymerizations, amidation, and reduction of metal ions, were performed on the functional CNTs, affording various CNT-polymer and CNT-Pt nanohybrids. The resulting materials were characterized by various measurements, such as TGA, Raman, XPS, FTIR, NMR, XRD, SEM, TEM, and HRTEM. The presented one-step methodology opens the avenue for industrial production of functional CNTs.
引用
收藏
页码:360 / 370
页数:11
相关论文
共 68 条
[1]   Covalent surface chemistry of single-walled carbon nanotubes [J].
Banerjee, S ;
Hemraj-Benny, T ;
Wong, SS .
ADVANCED MATERIALS, 2005, 17 (01) :17-29
[2]   A generic organometallic approach toward ultra-strong carbon nanotube polymer composites [J].
Blake, R ;
Gun'ko, YK ;
Coleman, J ;
Cadek, M ;
Fonseca, A ;
Nagy, JB ;
Blau, WJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (33) :10226-10227
[3]   Microwave-induced multiple functionalization of carbon nanotubes [J].
Brunetti, Fulvio G. ;
Herrero, M. Antonia ;
Munoz, Juan de M. ;
Diaz-Ortiz, Angel ;
Alfonsi, Jessica ;
Meneghetti, Moreno ;
Prato, Maurizio ;
Vazquez, Ester .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (25) :8094-8100
[4]   Etching of carbon nanotubes by ozone - A surface area study [J].
Byl, O ;
Liu, J ;
Yates, JT .
LANGMUIR, 2005, 21 (09) :4200-4204
[5]   ALIPHATIC AMINO AZIDES AS KEY BUILDING-BLOCKS FOR EFFICIENT POLYAMINE SYNTHESES [J].
CARBONI, B ;
BENALIL, A ;
VAULTIER, M .
JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (14) :3736-3741
[6]   Production and assessment of polycarbonate composites reinforced with vapour-grown carbon fibres [J].
Carneiro, OS ;
Covas, JA ;
Bernardo, CA ;
Caldeira, G ;
Van Hattum, FWJ ;
Ting, JM ;
Alig, RL ;
Lake, ML .
COMPOSITES SCIENCE AND TECHNOLOGY, 1998, 58 (3-4) :401-407
[7]   Solution properties of single-walled carbon nanotubes [J].
Chen, J ;
Hamon, MA ;
Hu, H ;
Chen, YS ;
Rao, AM ;
Eklund, PC ;
Haddon, RC .
SCIENCE, 1998, 282 (5386) :95-98
[8]   Amphiphilic cylindrical core-shell brushes via a "grafting from" process using ATRP [J].
Cheng, GL ;
Boker, A ;
Zhang, MF ;
Krausch, G ;
Müller, AHE .
MACROMOLECULES, 2001, 34 (20) :6883-6888
[9]  
Dujardin E, 1998, ADV MATER, V10, P1472, DOI 10.1002/(SICI)1521-4095(199812)10:17<1472::AID-ADMA1472>3.0.CO
[10]  
2-R