Ce3+-induced Fluorescence Amplification of Copper Nanoclusters Based on Aggregation-induced Emission for Specific Sensing 2,6-pyridine Dicarboxylic Acid

A straightforward, cost-effective and biocompatible reduction approach was applied to fabricate soluble but non-luminous glutathione-stabilized copper nanocluster (GSH-CuNCs). Surprisingly, as high as 1 × 10 3 times fluorescence enhancement was acquired when Ce 3+ was injected at an extremely low concentration of only 18 µM. Ce 3+ outperformed other rare-earth metal ions in terms of inducing fluorescence amplification of the non-luminous GSH-CuNCs. Furthermore, Ce 3+ was employed as inducer for aggregation-induce emission (AIE) effect as well as reactant to coordinate with target of 2,6-pyridine dicarboxylic acid (DPA) due to the stronger coordination ability between Ce 3+ and DPA than that of Ce 3+ and GSH. As a result, the Ce 3+ /GSH-CuNCs ensemble was developed as a novel sensor to detect DPA in the "on–off" mode. When DPA was introduced into the sensor, Ce 3+ failed to interact with GSH and detached from the surface of GSH-CuNCs, leading to fluorescence quenching. In addition, static quenching process and internal filtration effect (IFE) between Ce 3+ /GSH-CuNCs and DPA were also responsible for fluorescence quenching effect. A good linear relationship was obtained from 0.3 µM to 18 µM, with a limit of detection (LOD) of 0.19 µM. The as-proposed probe displayed high specificity to DPA and provided a simple, fast rapid and cheap method for construction this type of ensemble sensors to detect other targets.