Polymer Precursor Strategy Toward the Precise Synthesis of Uniform Hairy Carbon Dots with Tunable Sizes and Size Effects over Their Fluorescence

费斯特共振能量转移 荧光 聚合物 量子点 光化学 原子转移自由基聚合 猝灭(荧光) 聚合 共聚物 纳米技术 材料科学 化学 光学 物理 复合材料
作者
Chushu Huang,Meiran Feng,Xueer Zhu,Qinyu Zhou,Shanshan Zeng,Yifu Huang,Hefeng Zhang
出处
期刊:Macromolecules [American Chemical Society]
卷期号:54 (24): 11497-11507 被引量:13
标识
DOI:10.1021/acs.macromol.1c01766
摘要

A polymeric precursor strategy was developed toward precise synthesis of uniform and size-tunable hairy fluorescent carbon dots (C-dots, CDs). The strategy was achieved by (i) the synthesis of core–shell 6-arm starlike block copolymers of PGMA-b-PMMA (poly(glucosyl methyacrylate), PGMA; poly(methyl methacrylate), PMMA), serving as a precursor using atom transfer radical polymerization (ATRP) and (ii) selective carbonization of the inner PGMA chains to generate hairy C-dots with PMMA blocks attaching on the surfaces. The resultant C-dots with tunable sizes showed blue to green fluorescence depending on the excitation, size, and concentration. The large size of the C-dots led to a significant red shift of fluorescence emission, which was attributed to enhanced intra-C-dot Förster resonance energy transfer (FRET) between the emitter homologues in a single C-dot. In addition, the FRET effect between C-dots was further confirmed by the aggregation-caused quenching characteristics and red shift of emission at high concentrations. Interestingly, different from the traditional fluorophores with photobleaching characteristics, C-dots showed recoverable photoabsorption capacity and enhanced fluorescence after the long-time exposure to UV light.

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