首页> 外文期刊>Journal of the American Chemical Society >Quantum Beats in Crystalline Tetracene Delayed Fluorescence Due to Triplet Pair Coherences Produced by Direct Singlet Fission
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Quantum Beats in Crystalline Tetracene Delayed Fluorescence Due to Triplet Pair Coherences Produced by Direct Singlet Fission

机译:由于直接单线态裂变产生的三重态对相干性,晶体四烯延迟的荧光中的量子搏动。

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摘要

A detailed analysis of the oscillations seen in the delayed fluorescence of crystalline tetracene is presented in order to study the mechanism of singlet fission. Three quantum beat frequencies of 1.06 ± 0.05, 1.82 ± 0.05, and 2.92 ± 0.06 GHz are resolved, which are damped on a time scale of 20 ns. The effects of sample morphology, excitation wavelength, and temperature are examined. A density matrix model for singlet fission is developed that quantitatively describes the frequencies, amplitudes, and damping of the oscillations. The model assumes a direct coupling of the initially excited singlet exdton to the triplet pair manifold. There is no electronic coherence between the singlet and triplet pair states, but the rapid singlet decay time of ~200 ps in solution-grown single crystals provides the impulsive population transfer necessary to create a coherent superposition of three zero-field triplet pair states lxx>, lyy>, and lzz> with overall singlet character. This superposition of the three states gives rise to the three quantum beat frequencies seen in the experiment. Damping of the quantum beats results from both population exchange between triplet and singlet manifolds and pure dephasing between the triplet pair states. By lowering the temperature and slowing the SF rate, the visibility of the oscillations decreases. There is no evidence of magnetic dipole-dipole coupling between the product triplets. Our model provides good overall agreement with the data, supporting the conclusion that singlet fission in tetracene proceeds through the "direct" mechanism without strong electronic coupling between the singlet and triplet pair states.
机译:为了研究单重态裂变的机理,对晶体并四苯的延迟荧光中观察到的振荡进行了详细分析。解析了1.06±0.05、1.82±0.05和2.92±0.06 GHz的三个量子拍频,它们在20 ns的时间范围内被衰减。检查了样品形态,激发波长和温度的影响。建立了用于单重态裂变的密度矩阵模型,该模型定量描述了振动的频率,幅度和阻尼。该模型假定初始激发的单重态激态与三重态对歧管直接耦合。单线态和三线态对之间没有电子相干性,但是溶液生长的单晶中约200 ps的快速单线态衰减时间提供了创建三个零场三线态对态的相干叠加所必需的脉冲迁移。 ,lyy>和lzz>并带有整体单线字符。这三个状态的叠加产生了实验中看到的三个量子拍频。量子拍的阻尼是由于三重态和单重态流形之间的总体交换以及三重态对状态之间的纯相移。通过降低温度并降低SF速率,振荡的可见度降低。没有证据表明三胞胎之间存在磁偶极-偶极耦合。我们的模型与数据提供了良好的整体一致性,支持了并四苯碳体中的单重态裂变通过“直接”机制进行的结论,而在单重态和三重态对状态之间没有强电子耦合。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第20期|p.8597-8607|共11页
  • 作者单位

    Department of Chemistry, University of California, Riverside, 501 Big Springs Road, Riverside, California 92521, United States;

    Department of Chemistry, University of California, Riverside, 501 Big Springs Road, Riverside, California 92521, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:13:28

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