A Numerical Study of Lossy Multipole Debye Dispersive Media Using a Recursive Integral-FDTD Method

With high photoluminescence efficiency and a simple solution synthesis method, lead halide perovskites are expected to be a promising material for display and illumination. However, the toxicity and environmental sensitivity of lead hinder its potential applications. Here, we introduced Sb3+ ions into the lead-free perovskites derivative (NH4)(2)SnCl6 via a doping strategy. For the first time we synthesis the excitation-dependent perovskite with dynamically tunable fluorescence from yellow to near-infrared (NIR) emission by varying the UV excitation from 360 to 390 nm at room temperature. The DFT calculations are highly consistent no matter whether the coordination number of Sb3+ is 5 or 6. In contrasting to the early report of Sb triplet emission in the Sb doped perovskite, this material give a mixed self-trapped exciton (STE) emission. The 590 nm emission band is derived from the STE of SbCl5, and the 734 nm NIR emission band is attributed to the Sb-Sn mixed STE, which is supported by DFT calculations and spectral results. This study provides guidance for the design of perovskite phosphors with high efficiency and excitation-dependent properties.

Automated summary

By introducing Sb3+ ions into lead-free perovskite derivative (NH4)2SnCl6, the excitation-dependent perovskite with dynamically tunable fluorescence from yellow to near-infrared emission was synthesized for the first time. This study provides guidance for the design of perovskite phosphors with high efficiency and excitation-dependent properties.