材料科学
纳米纤维
碳纳米纤维
碳化
超分子化学
纤维
聚丙烯腈
化学工程
结晶度
石墨氮化碳
三聚氰酸
纳米技术
成核
复合材料
三聚氰胺
聚合物
晶体结构
有机化学
催化作用
化学
碳纳米管
工程类
光催化
扫描电子显微镜
作者
Ye Zhang,Bo Zhu,Shengyao Zhao,Wei Zhao,Mingzhe Zhou,Yonglian Sun,Kun Qiao,Jiani Liu,Jiaqi Zhou,Jialin Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-04-17
卷期号:18 (17): 11360-11374
被引量:1
标识
DOI:10.1021/acsnano.4c01161
摘要
The utilization of carbon-based fibers as a fundamental constituent holds strong appeal for diverse materials and devices. However, the poor fiber graphitic structure resulting from the heat treatment of atactic polyacrylonitrile (PAN) precursors often leads to a modest performance of carbon-based fibers. This paper takes electrospun carbon nanofibers (CNFs) as the research object and provides a seed-assisted graphitization strategy to improve the fiber graphitic structures. The typical melamine/cyanuric acid self-assembly precursor of graphitic carbon nitride is applied as supramolecular seeds in CNFs and demonstrates significant promotion of fiber graphitization, while it decomposes at elevated temperatures. Further studies show that the higher carbon content contributes to the better heat resistance of seeds; thus, nanoscale 2,6-diaminopyridine/cyanuric acid and 2,4,6-triaminopyrimidine/barbituric acid supramolecular seeds are developed. Both systems can be uniformly distributed in PAN precursors through in situ self-assembly and withstand high-temperature carbonization without severe pyrolysis. The dispersed seeds contribute to the formation of fibrillar PAN crystals and promote their conversion to ordered graphitic domains through nucleation and templating roles. The obtained CNFs exhibit increased crystallinity and graphitization degree with improved orientation and refined size of fiber crystals. As a result, the strength, modulus, and elongation at break of CNFs are comprehensively enhanced.
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