Rapid In Situ Polymerization of Polyacrylonitrile/Graphene Oxide Nanocomposites as Precursors for High-Strength Carbon Nanofibers

聚丙烯腈 材料科学 纳米纤维 碳纳米纤维 原位聚合 石墨烯 碳化 纳米复合材料 聚合 静电纺丝 复合材料 纳米技术 氧化物 化学工程 聚合物 碳纳米管 工程类 冶金 扫描电子显微镜
作者
Ye Zhang,Bo Zhu,Xun Cai,Xiaomin Yuan,Shengyao Zhao,Junwei Yu,Kun Qiao,Rongman Qin
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (14): 16846-16858 被引量:41
标识
DOI:10.1021/acsami.1c02643
摘要

Graphene oxide (GO) has been widely used as an additive of polyacrylonitrile (PAN)-based carbon nanofibers (CNFs) to optimize its crystal structure and improve the mechanical performances of nanofibers. However, the homogeneous dispersion of GO nanosheets among entangled PAN molecular chains is always challenging, and the poor dispersion of GO severely limits its positive effects on both the structure and performances of CNFs. Considering this issue, this paper provides for the first time an effective solution to achieve rapid and uniform introduction of GO in PAN-based nanofibers via in situ polymerization, and the optimization of the nanofiber structure by GO is systematically studied in three consecutive stages (polymerization, electrospinning, and carbonization) of the production process. During in situ polymerization, PAN is tightly attached on GO nanosheets to form PAN/GO nanocomposites, and this interaction is maintained throughout the spinning process. Not only the arrangement of PAN molecular chains but also the crystal size of the final turbostratic structure of CNFs is considerably improved by the interaction between PAN and GO. Besides, the direct proof that GO nanosheets promote the crystallization and orientation of the nanofiber matrix is presented. As a result, the tensile strength of CNFs is remarkably increased by 2.45 times with 0.5 wt % addition of GO. In summary, this paper provides a method for efficiently introducing nanoscale additives into PAN-based nanofibers and gives insights into the production of high-performance CNFs with the addition of GO.
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