Anion Exchanges of Water-Stable Perovskite Nanocrystals in the Pure Water Phase and Applications in Detecting Halide Ions via a Smartphone-Based Sensing Platform

Abstract

Recently, the newly emerging lead halide perovskite nanocrystals (PNCs) have been intensely researched in many fields, such as light-emitting diodes (LEDs), solar cells, lasers, and display devices. The extremely high fluorescence quantum yield (near 100%) of PNCs over classic fluorescent materials would enable good applications of PNCs in sensing. However, the study on PNCs for bio- and chemical sensing, especially for detecting targets that exist in aqueous medium, faces great challenges due to the well-known instability of PNCs in polar solvents, especially water. Although the encapsulation of polymers or inorganic materials can efficiently protect PNCs from decomposition in aqueous solution, the sensing based on the interaction between PNCs and targets is severely hindered by the compact protection coating at the surfaces of PNCs. In this work, novel water-dispersed PNCs (W-PNCs), i.e., CsPbBr 3 @CsPb 2 Br 5 PNCs, with strong fluorescence and excellent water stability were synthesized from OAm-capped CsPbBr 3 PNCs by a simple “oil–solid–water” phase transition. The W-PNCs without being encapsulated with compact polymers or inorganic materials can sensitively and stably sense targets in the pure water phase via direct chemical reactions. For the first time, ion exchanges between PNCs and halide ions and their effects on the fluorescence wavelength of PNCs were investigated in the pure water phase, on the basis of which a new, visualized, selective, and sensitive smartphone-based sensing platform for halide ions has been established by the integration of the conveniently prepared W-PNC nanoprobe and the portable mobile phone. It is envisioned that the uncoated but extremely water-stable and highly fluorescent W-PNCs have promising applications in chemical sensing, biosensing, and bioimaging of targets in aqueous medium.