偶氮苯
纳米纤维
材料科学
纳米技术
两亲性
光异构化
纳米材料
自组装
纳米尺度
纳米生物技术
聚合
聚合物
共聚物
纳米颗粒
催化作用
化学
有机化学
异构化
复合材料
作者
Haibao Jin,Pengchao Wu,Zhenghui Liu,Zichao Sun,Weisheng Feng,Yanhuai Ding,Huiliang Cao,Zhiqun Lin,Shaoliang Lin
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-08-02
卷期号:18 (32): 21576-21584
标识
DOI:10.1021/acsnano.4c08229
摘要
Ultrathin organic nanofibers (UTONFs) represent an emerging class of nanomaterials as they carry a set of favorable attributes, including ultrahigh specific surface area, lightweight, and mechanical flexibility, over inorganic counterparts, for use in biomedicine and nanotechnology. However, precise synthesis of uniform UTONFs (diameter ≤ 2 nm) with tailored functionalities remained challenging. Herein, we report robust multifunctional UTONFs using hydrophobic interaction-driven self-assembly of amphiphilic alternating peptoids containing hydrophobic photoresponsive azobenzene and hydrophilic hydroxyl moieties periodically arranged along the peptoid backbone. Notably, the as-crafted UTONFs are approximately 2 nm in diameter and tens of micrometers in length (an aspect ratio, AR, of ∼10000), exemplifying the UTONFs with the smallest diameter yielded via self-assembly. Intriguingly, UTONFs were disassembled into short-segmented nanofibers and controllably reassembled into UTONFs, resembling "step-growth polymerization". Photoisomerization of azobenzene moieties leads to reversible transformation between UTONFs and spherical micelles. Such meticulously engineered UTONFs demonstrate potential for catalysis, bioimaging, and antibacterial therapeutics. Our study highlights the significance of the rational design of amphiphiles containing alternating hydrophobic and hydrophilic moieties in constructing otherwise unattainable extremely thin UTONFs with ultrahigh AR and stimuli-responsive functionalities for energy and bionanotechnology.
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