Abstract

All-inorganic perovskite nanocrystals (NCs) exhibit great promise in optoelectronics and photovoltaics. However, their intrinsic low-thermal/oxygen/moisture stability and the rigorous synthesis procedures have limited the practical applications. Here, we present a facile, one-step, light-induced method to synthesize CsPbCl3:Mn2+ NCs at room temperature by using carbon tetrachloride (CCl4) as the halide source. The corresponding formation mechanism of CsPbCl3:Mn2+ NCs is revealed, where CsPbCl3:Mn2+ NCs are formed through the direct incorporation of [MnCl6]4− octahedral into the perovskite lattice during the nucleation and growth process. Additionally, we demonstrate the in-situ growth of CsPbCl3:Mn2+ NCs within mesoporous silica (mSiO2) spheres to form CsPbCl3:Mn2+@mSiO2 nanocomposites via the light-induced method, resulting in a remarkable improvement in high-temperature and long-time stability. As a prototype experiment, a white light-emitting diode (WLED) device is constructed using CsPbCl3:Mn2+@mSiO2 nanocomposites, which exhibits a bright white-light emission with the CIE chromaticity coordinate of (0.352, 0.340). It is anticipated that light-induced synthesis method provides a straightforward strategy for synthesizing multifunctional halide perovskite nanocrystals and nanocomposites for versatile applications.

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