<p>Excessive Cu<sup>2+</sup> levels pose severe threats to human health and ecosystems, necessitating sensitive and selective detection methods. A novel ratiometric fluorescent probe (CDs@RBH) based on fluorescence resonance energy transfer (FRET) was developed through electrostatic assembly. This nanoplatform employs carbon quantum dots (CDs) as the energy donor and rhodamine hydrazide (RBH) as the acceptor. Upon Cu<sup>2+</sup> addition, the spirolactam ring of RBH opens, triggering a distinct UV–Vis absorption peak at 550 nm, which overlaps with the emission spectrum of CDs (450 nm), enhancing FRET efficiency. This mechanism enables dual-signal readout: the fluorescence intensity of CDs at 450 nm decreases, while the RBH-Cu<sup>2+</sup> emission at 575 nm increases, allowing for precise ratiometric detection. The probe exhibits high selectivity and exceptional sensitivity, with a detection limit (LOD) of 0.65 μM and quantification limit (LOQ) of 2.09 μM. Practical applications in tap water samples demonstrate excellent recovery rates (96–108%). This work presents a straightforward synthesis method, environmental stability, and dual-channel signal verification for detection, making it a promising tool for real-world Cu<sup>2+</sup> monitoring in environmental and biological systems.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Construction of FRET-based CDs@RBH Ratiometric Fluorescent Probe for Cu2+ Sensing

  • Xuemei Dong,
  • Zhongfei Hu,
  • Xuan Xiao,
  • Keying Zhang,
  • Yujie Ding

摘要

Excessive Cu2+ levels pose severe threats to human health and ecosystems, necessitating sensitive and selective detection methods. A novel ratiometric fluorescent probe (CDs@RBH) based on fluorescence resonance energy transfer (FRET) was developed through electrostatic assembly. This nanoplatform employs carbon quantum dots (CDs) as the energy donor and rhodamine hydrazide (RBH) as the acceptor. Upon Cu2+ addition, the spirolactam ring of RBH opens, triggering a distinct UV–Vis absorption peak at 550 nm, which overlaps with the emission spectrum of CDs (450 nm), enhancing FRET efficiency. This mechanism enables dual-signal readout: the fluorescence intensity of CDs at 450 nm decreases, while the RBH-Cu2+ emission at 575 nm increases, allowing for precise ratiometric detection. The probe exhibits high selectivity and exceptional sensitivity, with a detection limit (LOD) of 0.65 μM and quantification limit (LOQ) of 2.09 μM. Practical applications in tap water samples demonstrate excellent recovery rates (96–108%). This work presents a straightforward synthesis method, environmental stability, and dual-channel signal verification for detection, making it a promising tool for real-world Cu2+ monitoring in environmental and biological systems.