磷光
系统间交叉
激子
材料科学
激发态
超快激光光谱学
量子产额
化学物理
光电子学
单重态
纳米技术
光化学
星团(航天器)
原子物理学
荧光
化学
光谱学
物理
光学
凝聚态物理
量子力学
计算机科学
程序设计语言
作者
Xuepeng Zhang,Lili Du,Weijun Zhao,Zheng Zhao,Yu Xiong,Xuewen He,Peng Fei Gao,Parvej Alam,Can Wang,Zhen Li,Jing Leng,Junxue Liu,Chuanyao Zhou,Jacky W. Y. Lam,David Lee Phillips,Guoqing Zhang,Ben Zhong Tang
标识
DOI:10.1038/s41467-019-13048-x
摘要
Purely organic room temperature phosphorescence (RTP) has attracted wide attention recently due to its various application potentials. However, ultralong RTP (URTP) with high efficiency is still rarely achieved. Herein, by dissolving 1,8-naphthalic anhydride in certain organic solid hosts, URTP with a lifetime of over 600 ms and overall quantum yield of over 20% is realized. Meanwhile, the URTP can also be achieved by mechanical excitation when the host is mechanoluminescent. Femtosecond transient absorption studies reveal that intersystem crossing of the host is accelerated substantially in the presence of a trace amount of 1,8-naphthalic anhydride. Accordingly, we propose that a cluster exciton spanning the host and guest forms as a transient state before the guest acts as an energy trap for the RTP state. The cluster exciton model proposed here is expected to help expand the varieties of purely organic URTP materials based on an advanced understanding of guest/host combinations.
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