Purely organic optoelectronic materials with ultralong-lived excited states under ambient conditions

激发态 磷光 材料科学 发光 光电子学 分子 纳米技术 工程物理 化学物理 原子物理学 化学 荧光 物理 光学 有机化学
作者
Jie Yuan,Yuting Tang,Shen Xu,Runfeng Chen,Wei Huang
出处
期刊:Science Bulletin [Elsevier BV]
卷期号:60 (19): 1631-1637 被引量:22
标识
DOI:10.1007/s11434-015-0894-9
摘要

The exponential growth of utilizing synthetic organic molecules in optoelectronic applications poses strong demands for rational control over the excited states of the materials. The manipulation of excited states through molecular design has led to the development of high-performance optoelectronic devices with tunable emission colors, high quantum efficiencies and efficient energy/charge transfer processes. Recently, a significant breakthrough in lifetime tuning of excited states has been made; the purely organic molecules were found to have ultralong-lived excited state under ambient conditions with luminescence lifetimes up to 1.35 s, which are several orders of magnitude longer than those of conventional organic fluorophores. Given the conceptual advance in understanding the fundamental behavior of excited state tuning in organic luminescent materials, the investigations of organic ultralong room-temperature phosphorescence (OURTP) should provide new directions for researches and have profound impacts on many different disciplines. Here, we summarized the recent understandings on the excited state tuning, the reported OURTP molecules and their design considerations, the spectacular photophysical performance, and the amazing optoelectronic applications of the newly emerged organic optoelectronic materials that free of heavy metals.
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