Effect of Chemical Modification of Graphene on Mechanical, Electrical, and Thermal Properties of Polyimide/Graphene Nanocomposites

被引:174
|
作者
Ha, Hun Wook [1 ]
Choudhury, Arup [1 ]
Kamal, Tahseen [1 ]
Kim, Dong-Hun [1 ]
Park, Soo-Young [1 ]
机构
[1] Kyungpook Natl Univ, Dept Polymer Sci & Engn, Taegu 702701, South Korea
基金
新加坡国家研究基金会;
关键词
nanocomposites; photoelectron spectroscopy (XPS); transmission electron microscopy (TEM); mechanical properties; thermal properties; electrical properties; GRAPHITE OXIDE; FILMS; SHEETS;
D O I
10.1021/am300999g
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Chemically modified graphene sheets were dispersed in a high-performance polyimide (PI) matrix using polyamic acid (PAA)/graphene nanocomposite as a precursor. PI nanocomposite films with different loadings of graphene sheets were prepared by thermal imidization of the as-prepared PAA/graphene nanocomposites. Graphene oxide (GO) synthesized by Hummer's method was chemically reduced with various reducing agents to produce reduced GOs (rGOs). The incorporation of only 5 wt % GO resulted in an similar to 12-fold and similar to 18-fold increase in the tensile strength and tensile modulus of PI, respectively, while the PI/rGO nanocomposites were found to have relatively inferior tensile properties. The superior mechanical properties of the PI/GO nanocomposites were attributed to the good dispersion and effective stress transfer between the polymer and GO sheets, as evidenced by the results from X-ray diffraction (XRD) and morphological studies. Furthermore, the PI/GO nanocomposites exhibited higher loading capacity than PI/rGO. The thermo-oxidative stability of PI was also remarkably improved with the addition of both GO and rGOs, but rGOs had a more pronounced effect. The electrical conductivity of PI/rGO nanocomposites was higher than that of PI/GO, suggesting restoration of the graphene basal plane upon the reduction of GO. The highest electrical conductivity was achieved for the L-ascorbic acid reduced GO-reinforced PI nanocomposites.
引用
收藏
页码:4623 / 4630
页数:8
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