Single-layer graphene nanosheets with controlled grafting of polymer chains

被引:397
作者
Fang, Ming [1 ]
Wang, Kaigang [1 ]
Lu, Hongbin [1 ]
Yang, Yuliang [1 ]
Nutt, Steven [2 ]
机构
[1] Fudan Univ, Dept Macromol Sci, Key Lab Mol Engn Polymers, Minist Educ, Shanghai 200433, Peoples R China
[2] Univ So Calif, Dept Chem Engn & Mat Sci, Los Angeles, CA 90089 USA
关键词
WALLED CARBON NANOTUBES; TRANSFER RADICAL POLYMERIZATION; GLASS-TRANSITION; GRAPHITE OXIDE; CHEMICAL FUNCTIONALIZATION; THERMAL-CONDUCTIVITY; RAMAN-SPECTROSCOPY; ORGANIC-SOLVENTS; HIGH-QUALITY; FILMS;
D O I
10.1039/b919078c
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
Single-layer graphene nanosheets (SLGNs) are prepared by reduction of well-exfoliated graphite oxide aided by a surfactant (sodium dodecylbenzene sulfonate, SDBS). Grafting density and polystyrene (PS) chain lengths are controlled by modulating the concentrations of diazonium compound and monomer during the grafting reaction of the initiator and the succeeding atomic transfer radical polymerization (ATRP). Atomic force microscopy (AFM), X-ray diffraction (XRD), Raman spectra and transmission electron microscopy (TEM) are used to confirm the single-layer structure of graphene sheets, covalent bonding at the interface, and distribution uniformity of grafting PS chains at the SLGN surface. Thermogravimetric analysis (TGA) is performed to assess the control of grafting density and chain length. PS chains grafted on the SLGN surface exhibited remarkably confined relaxation behavior. An increase in the glass transition temperature (T-g) of up to 18 degrees C is observed for high grafting density, low molecular weight polymer-grafted graphene samples. The low grafting density, high molecular weight sample shows an increase in T-g of similar to 9 degrees C, which is attributed to superior heat conduction efficiency. The measured thermal conductivity for the PS composite film with 2.0 wt% SLGNs increase by a factor of 2.6 compared to that of the pure PS.
引用
收藏
页码:1982 / 1992
页数:11
相关论文
共 75 条
[1]   Continuum Elastic Modeling of Graphene Resonators [J].
Atalaya, Juan ;
Isacsson, Andreas ;
Kinaret, Jari M. .
NANO LETTERS, 2008, 8 (12) :4196-4200
[2]   Non-covalent functionalization of graphene sheets by sulfonated polyaniline [J].
Bai, Hua ;
Xu, Yuxi ;
Zhao, Lu ;
Li, Chun ;
Shi, Gaoquan .
CHEMICAL COMMUNICATIONS, 2009, (13) :1667-1669
[3]   Nanoparticle polymer composites: Where two small worlds meet [J].
Balazs, Anna C. ;
Emrick, Todd ;
Russell, Thomas P. .
SCIENCE, 2006, 314 (5802) :1107-1110
[4]   Quantitative equivalence between polymer nanocomposites and thin polymer films [J].
Bansal, A ;
Yang, HC ;
Li, CZ ;
Cho, KW ;
Benicewicz, BC ;
Kumar, SK ;
Schadler, LS .
NATURE MATERIALS, 2005, 4 (09) :693-698
[5]   Chemical Modification of Epitaxial Graphene: Spontaneous Grafting of Aryl Groups [J].
Bekyarova, Elena ;
Itkis, Mikhail E. ;
Ramesh, Palanisamy ;
Berger, Claire ;
Sprinkle, Michael ;
de Heer, Walt A. ;
Haddon, Robert C. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (04) :1336-+
[6]  
Boukhvalov DW, 2008, NANO LETT, V8, P4373, DOI [10.1021/nl802234n, 10.1021/nl802098g]
[7]  
Brown M.E., 1998, Handbook of thermal analysis and calorimetry: principles and practice, V1
[8]   General equation for the determination of the crystallite size La of nanographite by Raman spectroscopy [J].
Cançado, LG ;
Takai, K ;
Enoki, T ;
Endo, M ;
Kim, YA ;
Mizusaki, H ;
Jorio, A ;
Coelho, LN ;
Magalhaes-Paniago, R ;
Pimenta, MA .
APPLIED PHYSICS LETTERS, 2006, 88 (16)
[9]  
Choucair M, 2009, NAT NANOTECHNOL, V4, P30, DOI [10.1038/nnano.2008.365, 10.1038/NNANO.2008.365]
[10]   Effect of changing polymer chain length on the target-mediated agglutination of polymer-grafted nanoparticles [J].
Costanzo, Philip J. ;
Dan, Nily ;
Lancaster, Katherine S. ;
Lebrilla, Carlito B. ;
Patten, Timothy E. .
MACROMOLECULES, 2008, 41 (04) :1570-1576