Synthesis of a water-stable fluorescence CsPbBr3 perovskite by dual-supersaturated recrystallization method and tuning the fluorescence spectrum for selective detection of folic acid

As an excellent fluorescent material, cesium lead halide perovskite nanocrystals (PNCs) is rarely used for analytical purposes because the PNCs are unstable in polar solvents, especially water. Developing a new synthesis method to prepare water-stable PNCs makes it promising for the detection of analytes in aqueous solutions. Herein, by using the solubility difference of the precursors in different solvents, we successfully synthesized water-stable CsPbBr3 PNCs by a dual-supersaturated recrystallization method at room temperature. We also found that the fluorescence of the as-prepared CsPbBr3 PNCs could be quenched by some small organic molecules, such as folic acid (FA) and dopamine (DA). By using a chloride-induced anion exchange reaction method, the fluorescence emission peak of the CsPbBr3 PNCs could be tuned from 518 to 418 nm and the emission color changed from green to blue. The blue emission chloride-exchanged PNCs have a good selectivity for only FA and a good linear relationship is established between the fluorescence quenching rate of the PNCs and concentration of FA from 10.0 to 140.0 μM, with a limit of detection (LOD) of 0.9 μM. This work expanded the applications of PNCs in the field of analytical chemistry and also proposed a new strategy for improving selectivity by tuning the emission spectrum of a fluorescent probe.