荧光
量子产额
生物相容性
光化学
蓝移
选择性
硫化镉
紫外线
碳纤维
化学
纳米颗粒
发光
材料科学
量子点
辐照
纳米技术
光致发光
光电子学
无机化学
复合数
光学
有机化学
催化作用
核物理学
复合材料
物理
作者
Yuwei Wang,Ye Li,Guang Yang,Xiao‐Jun Yang,Chenglu Yan,Huaqiao Peng,Jianji Wang,Juan Du,Baozhan Zheng,Youguang Guo
标识
DOI:10.1016/j.cclet.2023.108277
摘要
Carbon dots (CDs) have been attracted much attention and widely studied due to their excellent fluorescence (FL) properties, better biocompatibility and outstanding photo/chemical stability. However, the disadvantage of lower quantum yield (QY) still limits its wide application. Herein, we reported a novel and convenient strategy to prepare photo-induced Ag/CDs (p-Ag/CDs) by irradiating the mixed Ag+ and hydrophobic CDs (h-CDs) acetone solution with ultraviolet (UV) light. The obtained p-Ag/CDs exhibit a greatly enhanced FL emission together with a blue shift (460 nm) than h-CDs (520 nm). The QY of p-Ag/CDs is measured to be 51.1%, which is 10.4 times higher than that of h-CDs (4.9%), indicating that photo-induced Ag modulation can effectively improve the optical properties of CDs. The mechanisms for the FL enhancement and blue shift of h-CDs are studied in detail. The results prove that the greatly enhanced FL emission is from the generated Ag nanoparticles (AgNPs) by UV light irradiation based on metal-enhanced fluorescence (MEF), and the increased oxygen-contained groups in this process lead to the blue shift in CDs fluorescence. Interestingly, the p-Ag/CDs exhibit higher sensitivity and selectivity for sulfide ions (S2−) detection than that of h-CDs, which have a lower response to S2−. This work not only offers a novel strategy to improve the FL properties of materials but also endows them with new functions and broadens their application fields.
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