超快激光光谱学
光激发
准分子
化学
皮秒
光化学
激发态
光谱学
飞秒
ZSM-5型
红外光谱学
分析化学(期刊)
吸附
荧光
物理化学
原子物理学
激光器
分子筛
光学
有机化学
物理
量子力学
作者
Lucie Duplouy,M. Hureau,Aurélien Moncomble,Svetlana Mintova,Olivier Gardoll,Alain Moissette,V. De Waele
标识
DOI:10.1140/epjs/s11734-023-00813-9
摘要
The photo-physical properties of dicyanoanthracene (DCA) molecules adsorbed on the external surface of ZSM-5 zeolite, forming DCA@ZSM-5 composites, have been investigated by picosecond transient emission, femtosecond transient absorption infrared vibrational spectroscopy, steady-state UV–vis, and quantum chemistry calculations. Following the photoexcitation at 420 nm of DCA@ZSM-5, the formation of the localized, LE, excited S1 state of DCA emitting below 500 nm is observed. LE is rapidly and quasi-exclusively converted into two distinct exciplex species, EX1 and EX2, detected by their emission above 520 nm, with a lifetime of 5 ns and 20 ns, respectively. The different transient species can be identified by the frequency of the CN stretching vibration that is a marker of the charge delocalisation and that is peaking respectively at 2162 (LE), 2174 (EX1) and 2187 (EX2) cm−1. DFT and TD-DFT calculations further support the assignment. The results show that the external surface of zeolite is an appropriate playground for the development of novel photoactive host–guest materials.
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