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  1. Abstract

    The integration of highly luminescent CsPbBr3quantum dots on nanowire waveguides has enormous potential applications in nanophotonics, optical sensing, and quantum communications. On the other hand, CsPb2Br5nanowires have also attracted a lot of attention due to their unique water stability and controversial luminescent property. Here, the growth of CsPbBr3nanocrystals on CsPb2Br5nanowires is reported first by simply immersing CsPbBr3powder into pure water, CsPbBr3−γ Xγ(X = Cl, I) nanocrystals on CsPb2Br5−γ Xγnanowires are then synthesized for tunable light sources. Systematic structure and morphology studies, including in situ monitoring, reveal that CsPbBr3powder is first converted to CsPb2Br5microplatelets in water, followed by morphological transformation from CsPb2Br5microplatelets to nanowires, which is a kinetic dissolution–recrystallization process controlled by electrolytic dissociation and supersaturation of CsPb2Br5. CsPbBr3nanocrystals are spontaneously formed on CsPb2Br5nanowires when nanowires are collected from the aqueous solution. Raman spectroscopy, combined photoluminescence, and SEM imaging confirm that the bright emission originates from CsPbBr3−γ Xγnanocrystals while CsPb2Br5−γ Xγnanowires are transparent waveguides. The intimate integration of nanoscale light sources with a nanowire waveguide is demonstrated through the observation of the wave guiding of light from nanocrystals and Fabry–Perot interference modes of the nanowire cavity.

     
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