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Control of the Singlet–Triplet Energy Gap in a Thermally Activated Delayed Fluorescence Emitter by Using a Polar Host Matrix

机译:通过使用极性宿主矩阵控制热激活延迟荧光发射体中的单重态-三重态能隙

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摘要

The photoluminescence properties of a thermally activated delayed fluorescence emitter, 1,2-bis(carbazol-9-yl)-4,5-dicyanobenzene (2CzPN), doped in a host matrix consisting of 1,3-bis(9-carbazolyl)benzene and a polar inert molecule, camphoric anhydride (CA), in various concentrations have been investigated. It is found that the addition of CA stabilizes only the lowest singlet excited state (S1) of 2CzPN without changing the energy level of the lowest triplet excited state (T1), leading to a reduction in the energy gap between S1 and T1. The maximum reduction of energy gap achieved in this work has been determined to be around 65 meV from the shift of the fluorescence spectrum and the temperature dependence of the photoluminescence decay rate.
机译:掺杂在由1,3-双(9-咔唑基)组成的基质中的热活化延迟荧光发射剂1,2-双(咔唑-9-基)-4,5-二氰基苯(2CzPN)的光致发光特性已经研究了各种浓度的苯和极性惰性分子樟脑酐(CA)。发现添加CA仅稳定了2CzPN的最低单重态激发态(S1),而没有改变最低三重态激发态(T1)的能级,导致S1和T1之间的能隙减小。从荧光光谱的移动和光致发光衰减率的温度依赖性可以确定,在这项工作中实现的能隙最大减少量约为65meV。

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