磷光
余辉
发光
激发态
化学物理
三重态
材料科学
分子
相(物质)
激子
光化学
化学
纳米技术
荧光
原子物理学
光电子学
物理
光学
凝聚态物理
有机化学
伽马射线暴
天文
作者
Xin Shen,Wanhua Wu,Cheng Yang
出处
期刊:Molecules
[MDPI AG]
日期:2024-07-08
卷期号:29 (13): 3236-3236
被引量:1
标识
DOI:10.3390/molecules29133236
摘要
Organic room temperature afterglow (ORTA) can be categorized into two key mechanisms: continuous thermally activated delayed fluorescence (TADF) and room-temperature phosphorescence (RTP), both of which involve a triplet excited state. However, triplet excited states are easily quenched by non-radiative transitions due to oxygen and molecular vibrations. Solid-phase systems provide a conducive environment for triplet excitons due to constrained molecular motion and limited oxygen permeation within closely packed molecules. The stimulated triplet state tends to release energy through radiative transitions. Despite numerous reports on RTP in solid-phase systems in recent years, the complexity of these systems precludes the formulation of a universal theory to elucidate the underlying principles. Several strategies for achieving ORTA luminescence in the solid phase have been developed, encompassing crystallization, polymer host-guest doping, and small molecule host-guest doping. Many of these systems exhibit luminescent responses to various physical stimuli, including light stimulation, mechanical stimuli, and solvent vapor exposure. The appearance of these intriguing luminescent phenomena in solid-phase systems underscores their significant potential applications in areas such as light sensing, biological imaging, and information security.
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