• 文献标题:   Effect of Molecular Chain Length on the Mechanical and Thermal Properties of Amine-Functionalized Graphene Oxide/Polyimide Composite Films Prepared by In Situ Polymerization
  • 文献类型:   Article
  • 作  者:   LIAO WH, YANG SY, WANG JY, TIEN HW, HSIAO ST, WANG YS, LI SM, MA CCM, WU YF
  • 作者关键词:   graphene oxide, aminefunctionalized, polyimide, composite, in situ polymerization
  • 出版物名称:   ACS APPLIED MATERIALS INTERFACES
  • ISSN:   1944-8244 EI 1944-8252
  • 通讯作者地址:   Natl Tsing Hua Univ
  • 被引频次:   80
  • DOI:   10.1021/am302494c
  • 出版年:   2013

▎ 摘  要

This study fabricates amine (NH2)-functionalized graphene oxide (GO)/polyimide(PI) composite films with high performance using in situ polymerization. Linear poly(oxyalkylene)amines with two different molecular weights 400 and 2000 (D400 and D2000) have been grafted onto the GO surfaces, forming two types of NE12-functionalized GO (D400-GO/D2000-GO). NH2-functionalized GO, especially D400-GO, demonstrated better reinforcing efficiency in mechanical and thermal properties. The observed property enhancement are due to large aspect ratio of GO sheets, the uniform dispersion of the GO within the PI matrix, and strong interfacial adhesion due to the chemical bonding between GO and the polymeric matrix. The Young's modulus of the composite films with 0.3 wt % D400-GO loading is 7.4 times greater than that of neat PI, and tensile strength is 240% higher than that of neat PI. Compared to neat PI, 0.3 wt % D400-GO/PI film exhibits approximately 23.96 degrees C increase in glass transition temperature (T-g). The coefficient of thermal expansion below T-g is significantly decreased from 102.6 mu m/degrees C (neat PI) to 53.81 mu m/degrees C (decreasing 48%) for the D400-GO/PI composites with low D400-GO content (0.1 wt %). This work not only provides a method to develop the GO-based polyimide composites with superior performances but also conceptually provides a chance to modulate the interfacial interaction between GO and the polymer through designing the chain length of grafting molecules on NE12-functionalized GO.