Multiamino-functionalized carbon nanotubes and their applications in loading quantum dots and magnetic nanoparticles

被引:63
作者
Li, WW [1 ]
Gao, C [1 ]
Qian, HF [1 ]
Ren, JC [1 ]
Yan, DY [1 ]
机构
[1] Shanghai Jiao Tong Univ, Coll Chem & Chem Engn, Shanghai 200240, Peoples R China
关键词
D O I
10.1039/b600190d
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
Two strategies were employed to synthesize amino-functionalized multiwalled carbon nanotubes (MWNTs). In the first strategy, we grew poly(2-dimethylaminoethyl methacrylate) ( PDMAEMA) from the surfaces of MWNTs by in situ atom transfer radical polymerization ( ATRP), then allowed the polymer chains to react with methyl iodide to acquire cationic polyamine coated-carbon nanotubes (MWNT-PAmMeI). Three samples with different amounts of grafted polyamine were obtained. TGA measurements showed that the content of PDMAEMA was ca. 25, 60 and 80% by mass. The chemical structure, morphology and nanostructures of the polyamine-grafted MWNTs were confirmed by H-1 NMR spectroscopy, SEM and TEM. In the second strategy, we prepared amino-functionalized MWNTs (MWNT-NH2) by reacting acyl chloride-containing MWNTs with para-phenylenediamine in the presence of pyridine. The resulting polyamine- and amino-functionalized MWNTs were then used as templates to load CdTe quantum dots (QDs) and Fe3O4 magnetic nanoparticles by the electrostatic self-assembly approach, affording MWNT/CdTe and MWNT/Fe3O4 nanohybrids. TEM, EDS and XRD showed the structure and components of the obtained nanohybrids. Luminescence measurements indicated that the MWNT/CdTe complexes based on MWNT-PAmMeI could retain the luminescent properties of the QDs, which showed an emission peak at a wavelength of 550 nm, while the photoluminescence (PL) of the MWNT-NH2/CdTe composites can be hardly detected.
引用
收藏
页码:1852 / 1859
页数:8
相关论文
共 68 条
[21]   Photoluminescence quenching control in quantum dot-carbon nanotube composite colloids using a silica-shell spacer [J].
Grzelczak, M ;
Correa-Duarte, MA ;
Salgueiriño-Maceira, V ;
Giersig, M ;
Diaz, R ;
Liz-Marzán, LM .
ADVANCED MATERIALS, 2006, 18 (04) :415-+
[22]   A direct route toward assembly of nanoparticle-carbon nanotube composite materials [J].
Han, L ;
Wu, W ;
Kirk, FL ;
Luo, J ;
Maye, MM ;
Kariuki, NN ;
Lin, YH ;
Wang, CM ;
Zhong, CJ .
LANGMUIR, 2004, 20 (14) :6019-6025
[23]   Attachment of single CdSe nanocrystals to individual single-walled carbon nanotubes [J].
Haremza, JM ;
Hahn, MA ;
Krauss, TD .
NANO LETTERS, 2002, 2 (11) :1253-1258
[24]   Functionalization of carbon nanotubes with polystyrene [J].
Hill, DE ;
Lin, Y ;
Rao, AM ;
Allard, LF ;
Sun, YP .
MACROMOLECULES, 2002, 35 (25) :9466-9471
[25]   Synthesis and characterization of CdS/multiwalled carbon nanotube heterojunctions [J].
Huang, Q ;
Gao, L .
NANOTECHNOLOGY, 2004, 15 (12) :1855-1860
[26]   HELICAL MICROTUBULES OF GRAPHITIC CARBON [J].
IIJIMA, S .
NATURE, 1991, 354 (6348) :56-58
[27]   Atom transfer radical block copolymerization of 2-(N,N-dimethylamino)ethyl methacrylate and 2-hydroxyethyl methacrylate [J].
Jin, XP ;
Shen, YQ ;
Zhu, SP .
MACROMOLECULAR MATERIALS AND ENGINEERING, 2003, 288 (12) :925-935
[28]   Interparticle electron transfer in metal/semiconductor composites. Picosecond dynamics of CdS-capped gold nanoclusters [J].
Kamat, PV ;
Shanghavi, B .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (39) :7675-7679
[29]   Controlled functionalization of multiwalled carbon nanotubes by in situ atom transfer radical polymerization [J].
Kong, H ;
Gao, C ;
Yan, DY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (02) :412-413
[30]   Polyelectrolyte-functionalized multiwalled carbon nanotubes: preparation, characterization and layer-by-layer self-assembly [J].
Kong, H ;
Luo, P ;
Gao, C ;
Yan, D .
POLYMER, 2005, 46 (08) :2472-2485