摘要
Background Trace water contamination in organic solvents severely hampers chemical synthesis, pharmaceutical manufacturing, and electronic device fabrication; however, existing detection methods lack portability, adequate sensitivity, or stability. While MOF-based fluorescent sensors show promise, most are limited by single-signal outputs, weak anti-interference capability, and poor solvent tolerance. Results To address these challenges, we report an amino-functionalized europium-doped zirconium MOF (Eu@MOF-NH 2 ), synthesized via a one-step solvothermal method, serving as a robust ratiometric fluorescent probe for trace water detection. The material exhibits dual emissions: ligand-based (435 nm) and Eu 3+ -centered (614 nm). Upon water exposure, strong hydrogen bonds with the ligand activate intramolecular charge transfer (ICT) to intensify the blue emission. Concurrently, high-frequency O–H vibrational coupling quenches the red emission by blocking ligand-to-metal energy transfer, causing a rapid (<30 s) pink-to-blue visual transition. The fluorescence intensity ratio (I 435 /I 614 ) demonstrates excellent linearity with water content (0–10% v/v) and achieves ultralow limits of detection in ethanol (0.1643%), THF (0.0311%), methanol (0.3355%), and acetonitrile (0.0148%). Furthermore, this probe maintains consistent sensing performance across 11 diverse organic solvents with highly varying polarities. Integrated with a smartphone-assisted RGB colorimetric platform based on the blue-to-red intensity ratio, Eu@MOF-NH 2 enables portable, on-site, and quantitative visual detection. Significance This work overcomes the traditional limitations of sensitivity and stability, providing reliable material design and sensing strategies for industrial trace water monitoring and quality control.
危险品化学品经营许可证(带存储)