卤化物
纳米晶
纳米棒
铜
金属卤化物
激子
胶体
材料科学
光电效应
纳米技术
量子点
发光
无机化学
铯
化学
光电子学
物理化学
物理
凝聚态物理
冶金
作者
Pengfei Cheng,Lei Sun,Feng Lu,Songqiu Yang,Yang Yang,Daoyuan Zheng,Yang Zhao,Youbao Sang,Ruiling Zhang,Donghui Wei,Wei Deng,Keli Han
标识
DOI:10.1002/anie.201909129
摘要
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 CsCu2 I3 nanorods and 0D Cs3 Cu2 I5 NCs can be prepared. Density functional theory indicates that the reduced dimensionality in 1D CsCu2 I3 compared to 0D Cs3 Cu2 I5 makes the excitons more localized, which accounts for the strong emission of 0D Cs3 Cu2 I5 NCs. Subsequent optical characterization reveals that the highly luminescent, strongly Stokes-shifted broadband emission of 0D Cs3 Cu2 I5 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 Cs3 Cu2 I5 NCs in optoelectronics.
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