费斯特共振能量转移
荧光
光致发光
光化学
量子点
接受者
化学
材料科学
量子产额
兴奋剂
分析化学(期刊)
纳米技术
光电子学
有机化学
光学
物理
凝聚态物理
作者
Xun Zhou,Juerui Zhang,Dongyan Huang,Yinhui Yi,Kechen Wu,Gangbing Zhu
标识
DOI:10.1016/j.saa.2023.122484
摘要
In this work, a ratiometric fluorescence sensing platform was established to detect Cu2+ and D-PA (d-penicillamine) based on nitrogen-doped Ti3C2 MXene quantum dots (N-MODs) that was prepared via a simple hydrothermal method and exhibited strong fluorescent and photoluminescence performance as well as excellent stability. Since the oxidation reaction between o-phenylenediamine (OPD) and Cu2+ induced the formation of 2,3-diaminophenazine (ox-OPD) which not only can emerge an emission peak at 570 nm, but also inhibit the fluorescence intensity of N-MQDs at 450 nm, a ratiometric reverse fluorescence sensor via fluorescence resonance energy transfer (FRET) was designed to sensitively detect Cu2+, where N-MQDs acted as energy donor and ox-OPD as energy acceptor. More importantly, another considerably interesting phenomenon was that their catalytic oxidation reaction can be restrained in the presence of D-PA because of the coordination of Cu2+ with D-PA, further triggering the obvious changes in ratio fluorescent signal and color, thus a ratiometric fluorescent sensor of determining D-PA was proposed also in this work. After optimizing various conditions, the ratiometric sensing platform showed rather low detection limits for Cu2+ (3.0 nM) and D-PA (0.115 μM), coupled with excellent sensitivity and stability.
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