首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Investigation of Thermally Activated Delayed Fluorescence from a Donor-Acceptor Compound with Time-Resolved Fluorescence and Density Functional Theory Applying an Optimally Tuned Range-Separated Hybrid Functional
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Investigation of Thermally Activated Delayed Fluorescence from a Donor-Acceptor Compound with Time-Resolved Fluorescence and Density Functional Theory Applying an Optimally Tuned Range-Separated Hybrid Functional

机译:用时间分辨荧光和密度泛函理论的供体受体化合物的热活化延迟荧光的研究应用了最佳调整范围分离的混合功能

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摘要

Emitters showing thermally activated delayed fluorescence (TADF) in electroluminescent devices rely on efficient reverse intersystem crossing (rISC) arising from small thermal activation barriers between the lowest excited triplet and singlet manifolds. A small donor-acceptor compound consisting of a demethylacridine donor and a methylbenzoate acceptor group is used as a model TADF emitter. The spectroscopic signatures of this system are characterized using a combination of photoluminescence and photoluminescence excitation, and the photoluminescence decay dynamics are recorded between delays of 2 ns and 20 ms. Above T = 200 K, our data provide convincing evidence for TADF at intermediate delays in the microsecond range, whereas triplet-triplet annihilation and slow triplet decay at later times can be observed over the entire temperature range from T = 80 K to room temperature. Moreover, close to room temperature, we find a second and faster up-conversion mechanism, tentatively assigned to reverse internal conversion between different triplet configurations. An interpretation of these experimental findings requires a calculation of the deformation patterns and potential minima of several electronic configurations. This task is performed with a range-separated hybrid functional, outperforming standard density functionals or global hybrids. In particular, the systematic underestimation of the energy of charge transfer (CT) states with respect to local excitations within the constituting chromophores is replaced by more reliable transition energies for both kinds of excitations. Hence, several absorption and emission features can be assigned unambiguously, and the observed activation barriers for rISC and reverse internal conversion correspond to calculated energy differences between the potential surfaces in different electronic configurations.
机译:发射器表示电致发光器件热活化延迟荧光(TADF)依赖于从最低激发三重态和单歧管之间的小的热活化的障碍引起的有效的反向系间窜越(RISC)。由demethylacridine供体和甲基苯甲酸酯受体基团的一小施主 - 受主化合物被用作模型TADF发射极。该系统的光谱特征是使用的光致发光和光致发光激发的组合,其特征在于,与所述光致发光衰变动力学被记录的2纳秒和20ms的延迟之间。上述T = 200 K,我们的数据提供令人信服的证据TADF在微秒范围内的中间的延迟,而三重态 - 三重态湮灭和慢三重态衰变在稍后的时间可以在整个温度范围内从T = 80 K至室温进行观察。此外,接近室温,我们发现第二和更快的上变换机构,姑且被分配给反向不同三重构造之间内部转换。这些实验结果的解释需要变形模式和若干电子配置的潜在最小值的计算。该任务是与一系列分隔混合功能的执行,表现优于标准密度泛函或全球杂种。特别是,电荷转移的能量(CT)的系统性低估相对于所述发色团构成内本地激励是通过更可靠的跃迁能量为这两种激励状态代替。因此,若干的吸收和发射特征可以明确地分配,和用于RISC所观察到的活化障碍和反向内部转换对应于在不同的电子配置的电势面之间计算的能量差异。

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