摘要
The commercial applications of lead halide perovskites are limited by their adverse environmental hazards and intrinsic instability. One promising strategy to mitigate the Pb 2+ content is the doping of X 2+ transition metal ions into cesium lead halide CsPbX 3 (where X = Cl, Br, I) perovskite nanocrystals (PNCs). In this study, an ultrafast high-power ultrasonic synthesis method is employed to ensure uniform nucleation and growth of co-doped (Zn, Mn): CsPbCl 3 PNCs. Various analytical techniques are utilized to investigate the phase purity, microstructure, chemical composition, and photo-luminescence properties of the co-doped PNCs. Density functional theory (DFT) calculations reveal that the significantly enhanced optical performance of co-doped (Zn, Mn): CsPbCl 3 PNCs is primarily due to the increased formation energy resulting from the successful incorporation of Zn 2+ into Mn-doped CsPbCl 3 PNCs, without introducing new defect states. Additionally, the co-doped (Zn, Mn): CsPbCl 3 PNCs exhibit high sensitivity and selectivity in detecting Cu 2+ ions. Our findings propose a novel approach for tuning the optical properties of co-doped (Zn, Mn): CsPbCl 3 PNCs, highlighting their potential for applications in fluorescence sensors.
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