超细纤维
静电纺丝
聚丙烯腈
纳米纤维
共价键
多孔性
材料科学
制作
气凝胶
纤维
纳米技术
化学工程
复合材料
聚合物
化学
有机化学
工程类
医学
替代医学
病理
作者
Chengming Xiao,Yiyuan Yao,Xin Guo,Junwen Qi,Zhigao Zhu,Yujun Zhou,Yue Yang,Jiansheng Li
出处
期刊:Small
[Wiley]
日期:2024-02-19
被引量:4
标识
DOI:10.1002/smll.202311881
摘要
Abstract Shaping covalent organic frameworks (COFs) into macroscopic objects with robust mechanical properties and hierarchically porous structure is of great significance for practical applications but remains formidable and challenging. Herein, a general and scalable protocol is reported to prepare ultralight and robust pure COF fiber aerogels (FAGs), based on the epitaxial growth synergistic assembly (EGSA) strategy. Specifically, intertwined COF nanofibers (100–200 nm) are grown in situ on electrospinning polyacrylonitrile (PAN) microfibers (≈1.7 µm) containing urea‐based linkers, followed by PAN removal via solvent extraction to obtain the hollow COF microfibers. The resultant COF FAGs possess ultralow density (14.1–15.5 mg cm −3 ) and hierarchical porosity that features both micro‐, meso‐, and macropores. Significantly, the unique interconnected structure composed of nanofibers and hollow microfibers endows the COF FAGs with unprecedented mechanical properties, which can fully recover at 50% strain and be compressed for 20 cycles with less than 5% stress degradation. Moreover, the aerogels exhibit excellent capacity for organic solvent absorption (e.g., chloroform uptake of >90 g g −1 ). This study opens new avenues for the design and fabrication of macroscopic COFs with excellent properties.
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