发光
激发
材料科学
化学
分析化学(期刊)
原子物理学
光电子学
物理
色谱法
量子力学
作者
Guangkuo Dai,Zhimin Ma,Yixin Qiu,Zewei Li,Xiaohua Fu,Hong Jiang,Zhiyong Ma
标识
DOI:10.1021/acs.jpclett.2c01561
摘要
Herein, we report a novel hybrid organic–inorganic Zr(IV) metal halide ((CH3)4N)2ZrCl6, which demonstrates fascinating excitation-dependent luminescence across the full visible region. The single crystal of ((CH3)4N)2ZrCl6 showed an unexpected high degree of symmetry and formed a unique 0D structure with isolated [ZrCl6]2– octahedrons. Amazingly, three different emission groups emerged under changeable excitation light. The first emission group peaked at 462 nm with a ns lifetime and a μs lifetime, which is assigned to free-exciton fluorescence and thermally activated delayed fluorescence (TADF). The second group of emissions featured elaborate multipeak light-emitting components, which is ascribed to the d–d transitions of Zr(IV). The third emission group centered at 660 nm was attributed to the typical self-trapped exciton (STE) emission. To our best knowledge, this work for the first time reports a 0D organic–inorganic metal halide with distinctive excitation-dependent full-visible-spectrum luminescence via four different emission mechanisms.
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