三种状态蒽的三重态吸收性质研究
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作者单位:

1.中国科学院上海高等研究院;2.中国科学院大学;3.上海科技大学物质科学与技术学院

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中图分类号:

G633.7;O411.3

基金项目:

上海市科学技术委员会项目(20DZ2210300).


Study on the triplet state absorption properties of three states of anthracene
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Affiliation:

1.Shanghai Advanced Research Institute,Chinese Academy of Sciences;2.University of Chinese Academy of Sciences;3.School of Physical Science and Technology,ShanghaiTech University

Fund Project:

Science and Technology Commission of Shanghai Municipality (20DZ2210300)

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    摘要:

    利用瞬态吸收光谱技术研究蒽在甲苯溶液和PMMA薄膜及晶体的瞬态吸收过程,发现激发波长375 nm处的吸收度为0.7时,溶液中蒽的三重态最大吸收信号强度为其在PMMA中的5倍,而在高吸收度的晶体中,三重态吸收较低。通过建立模型分析,PMMA中的蒽分子存在光场诱导下偶极矩的宏观统计极化,导致宏观极化偶极矩的降低,而处于甲苯溶液中的蒽分子则易被光场所极化,产生较大的极化偶极矩,这是引起三重态吸收信号差异的原因。晶体状态下,S1能级发生分裂,低于T2能级,S1–T1能量差较大,系间窜越不有效,抑制了三重态吸收。以上结果解释了蒽分子在不同状态下三重态最大吸收信号差异。

    Abstract:

    The transient absorption process of anthracene in toluene solution, PMMA film and crystal was studied by transient absorption spectroscopy. It was found that when the absorption was 0.7 at the excitation wavelength of 375 nm, the maximum absorption signal intensity of the triplet state of anthracene in solution was five times that in PMMA. In the crystal with high absorption, the triplet state absorption signal is lower. By establishing a model, it was found that the anthracene molecules in PMMA exhibited macroscopic statistical polarization of the induced dipole moment under the optical field, resulting in a decrease in macroscopic polarization dipole moments. On the other hand, the anthracene molecules in the toluene solution were easily polarized by the optical field, resulting in a larger polarized dipole moment. This is the reason for the difference in triplet state absorption signals. In the crystal state, the S1 splits and is lower than T2. The energy gap between S1 and T1 is large, and the intersystem crossing is not effective, which inhibits the absorption of the triplet state. These results explain the difference in the maximum absorption signal of the triplet state of anthracene in different states.

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  • 收稿日期:2023-05-19
  • 最后修改日期:2023-05-19
  • 录用日期:2023-06-02
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