磷光
发光
结晶
猝灭(荧光)
分子
聚集诱导发射
材料科学
光化学
激发态
有机分子
化学物理
纳米技术
化学
荧光
光电子学
有机化学
原子物理学
光学
物理
作者
Elena Lucenti,Alessandra Forni,Chiara Botta,Lucia Carlucci,Clelia Giannini,Daniele Marinotto,Andrea Previtali,Stefania Righetto,Elena Cariati
标识
DOI:10.1021/acs.jpclett.7b00503
摘要
Solid-state luminescent materials with long lifetimes are the subject of ever-growing interest from both a scientific and a technological point of view. However, when dealing with organic compounds, the achievement of highly efficient materials is limited by aggregation-caused quenching (ACQ) phenomena on one side and by ultrafast deactivation of the excited states on the other. Here, we report on a simple organic molecule, namely, cyclic triimidazole (C9H6N6), 1, showing crystallization-induced emissive (CIE) behavior and, in particular, ultralong phosphorescence due to strong coupling in H-aggregated molecules. Our experimental data reveal that luminescence lifetimes up to 1 s, which are several orders of magnitude longer than those of conventional organic fluorophores, can be realized under ambient conditions, thus expanding the class of organic materials for phosphorescence applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI