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Abstract Low‐dimensional metal halides have recently attracted extensive attention owing to their unique structure and photoelectric properties. Herein, we report the colloidal synthesis of all‐inorganic low‐dimensional cesium copper halide nanocrystals (NCs) by adopting a hot‐injection approach. Using the same reactants and ligands, but different reaction temperatures, both 1D CsCu 2 I 3 nanorods and 0D Cs 3 Cu 2 I 5 NCs can be prepared. Density functional theory indicates that the reduced dimensionality in 1D CsCu 2 I 3 compared to 0D Cs 3 Cu 2 I 5 makes the excitons more localized, which accounts for the strong emission of 0D Cs 3 Cu 2 I 5 NCs. Subsequent optical characterization reveals that the highly luminescent, strongly Stokes‐shifted broadband emission of 0D Cs 3 Cu 2 I 5 NCs arises from the self‐trapped excitons. Our findings not only present a method to control the synthesis of low‐dimensional cesium copper halide nanocrystals but also highlight the potential of 0D Cs 3 Cu 2 I 5 NCs in optoelectronics.
Cheng et al. (Wed,) studied this question.
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