激发
激子
金属卤化物
卤化物
宽带
氯化铅
材料科学
密度泛函理论
化学物理
光电子学
化学
分子物理学
氯化物
光学
物理
凝聚态物理
无机化学
计算化学
冶金
量子力学
作者
Guanhong Wu,Chenkun Zhou,Wenmei Ming,Dan Han,Shiyou Chen,Dong Yang,Tiglet Besara,Jennifer Neu,Theo Siegrist,Mao‐Hua Du,Biwu Ma,Angang Dong
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-05-23
卷期号:3 (6): 1443-1449
被引量:144
标识
DOI:10.1021/acsenergylett.8b00661
摘要
Organic–inorganic metal halide hybrids have emerged as a new class of materials with fascinating optical and electronic properties. The exceptional structure tunability has enabled the development of materials with various dimensionalities at the molecular level, from three-dimensional (3D) to 2D, 1D, and 0D. Here, we report a new 1D lead chloride hybrid, C4N2H14PbCl4, which exhibits unusual inverse excitation-dependent broadband emission from bluish-green to yellow. Density functional theory calculations were performed to better understand the mechanism of this excitation-dependent broadband emission. This 1D hybrid material is found to have two emission centers, corresponding to the self-trapped excitons (STEs) and vacancy-bound excitons. The excitation-dependent emission is due to different populations of these two types of excitons generated at different excitation wavelengths. This work shows the rich chemistry and physics of organic–inorganic metal halide hybrids and paves the way to achieving novel light emitters with excitation-dependent broadband emissions at room temperature.
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