Deep-red ultralong room temperature phosphorescence of chitosan-based nanofibrous membrane activated by carboxylic acids

磷光 壳聚糖 纳米纤维 聚丙烯腈 化学工程 聚乙二醇 离子液体 材料科学 纺纱 聚合物 化学 高分子化学 纳米技术 有机化学 催化作用 荧光 物理 工程类 量子力学 生物化学
作者
Yifeng Cao,Kaimin Zhang,Haiyang Wang,Siyang Jiang,Faxu Lin,Danman Guo,Yuanchao Li,Huahua Huang,Zhiyong Yang,Zhenguo Chi
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:476: 146781-146781 被引量:27
标识
DOI:10.1016/j.cej.2023.146781
摘要

Organic non-conjugated materials with room temperature phosphorescence (RTP) have attracted increasing attention due to their fundamental importance and advantages like environmental friendliness, good biocompatibility, and various processing methods. However, most non-conjugated systems often suffered from the problem with very short RTP lifetimes in ambient conditions. Here, we proposed an efficient strategy to improve the RTP performance of chitosan (CTS) by constructing a strong ionic bond network based on carboxylic acids. The CA/CTS film prepared using citric acid (CA) as a solvent was found to emit a bright afterglow of about 5 s with a phosphorescence lifetime of up to 515 ms at 530 nm. Our experimental results indicated that forming synergistic networks of ionic and hydrogen bonding was a highly efficient method for achieving persistent RTP of CTS itself. Furthermore, due to the strong ionic interaction between 1-pyrenecarboxylic acid (PCA) and CTS, the PCA@CTS nanofibrous membrane with bright deep-red afterglow was first achieved through an electrostatic spinning technique using polyethylene glycol (PEG) or polyvinyl alcohol (PVA) as a co-spinning agent. This work not only offered a new kind of persistent RTP nanofibrous membrane but also gained a deeper insight into improving the phosphorescence properties of non-conjugated materials, especially natural polysaccharide.
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