系统间交叉
发光
材料科学
分子间力
化学物理
持续发光
荧光
分子
磷光
化学
纳米技术
光化学
单重态
光电子学
原子物理学
光学
热释光
物理
有机化学
激发态
作者
Zheng Wang,Cheng‐Yi Zhu,Zhang‐Wen Wei,Yanan Fan,Mei Pan
标识
DOI:10.1021/acs.chemmater.9b04440
摘要
Long persistent luminescence (LPL) materials have been fascinating from ancient times till today, whereas the generation and modulation of LPL are still uncontrollable in most cases. In this paper, a smart responsive metal–organic framework (MOF, LIFM-WZ-1) was reported to combine resilient structural dynamics with reversible LPL modulation. At room temperature in air, the as-prepared LIFM-WZ-1 has a staggered packing structure with inhaled water molecules between cavities, exhibiting fluorescence (F)-dominated blue emission. Under vacuum or by mild heating, the water molecules can be exhaled by the lattice, resulting in a crystal structure (LIFM-WZ-1a) with a reduced a axis and intensified intermolecular interactions. This brings transition to green excimer (E) emission related with lowered energy states. Meanwhile, orange-colored room temperature phosphorescence (RTP) is also enhanced, giving an overall balanced F/E/RTP emission. More fascinatingly, red LPL is ignited in the dehydrated sample, which is dumb in the original LIFM-WZ-1 because of intensified singlet to triplet intersystem crossing, damped high-energy oscillation, and compatible heat dissipation. The above breathing-induced LPL turn-on process is reversible by facile cooling, exposing to wet air, or purging in water vapor. This constitutes a successful exemplification in modulating LPL by the dynamic MOF, which provides potential applications in sensing, anti-counterfeiting, display, and so on.
科研通智能强力驱动
Strongly Powered by AbleSci AI