首页> 外文期刊>The Journal of Chemical Physics >TEMPERATURE DEPENDENCE OF OPTICAL DEPHASING IN AN ORGANIC POLYMER GLASS (PMMA) FROM 300 K TO 30 K
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TEMPERATURE DEPENDENCE OF OPTICAL DEPHASING IN AN ORGANIC POLYMER GLASS (PMMA) FROM 300 K TO 30 K

机译:300 K至30 K的有机聚合物玻璃(PMMA)中光脱色的温度依赖性

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The temperature dependence of the optical dephasing mechanism in an organic polymer glass, polymethylmethacrylate (PMMA), was studied from 300 K to 30 K using the dye IR144 as a probe. Transient grating and three pulse photon echo measurements were made, and the three pulse photon echo peak shift (3PEPS) was recorded as a function of temperature. The peak shift data reveal time constants of similar to 6 fs and similar to 60 fs, along with vibrational beats and a long-time constant value for the peak shift. The 6 fs component is attributed to intramolecular vibrations and the 60 fs component to librational degrees of freedom of the PMMA itself. This contribution appears slightly underdamped and the fitted spectral density matches well with the Raman spectrum of PMMA. The two ultrafast decays are insensitive to temperature. For temperatures above 80 K the long-time peak shift increases linearly as temperature decreases but at 80 K the shift levels off and decreases for temperatures between 80 and 30 K. Fit values for the inhomogeneous width (500 cm(-1)) and the reorganization energy (378 cm(-1)) describe the initial value of the peak shift, its decay, the absorption spectrum, and the three-pulse photon echo signal quite well at both high and low temperature. We were not very successful in describing the temperature dependence of the long-time peak shift, although the insensitivity of the dynamics to temperature could be qualitatively accounted for. At low temperature the imaginary portion of the line shape function, which is temperature independent, contributes significantly to the response, while at high temperature the dephasing is dominated by the real part of the line shape function. A more sophisticated model is required to quantitatively describe the data. (C) 1997 American Institute of Physics. [References: 58]
机译:使用染料IR144作为探针,研究了有机聚合物玻璃聚甲基丙烯酸甲酯(PMMA)中光学移相机理的温度依赖性,其范围为300 K至30K。进行了瞬态光栅和三个脉冲光子回波的测量,并记录了三个脉冲光子回波峰位移(3PEPS)与温度的关系。峰位移数据揭示了类似于6 fs和类似于60 fs的时间常数,以及振动跳动和峰位移的长时间常数。 6 fs分量归因于分子内振动,而60 fs分量归因于PMMA本身的自由自由度。这种贡献似乎略有不足,并且拟合的光谱密度与PMMA的拉曼光谱非常匹配。这两个超快衰减对温度不敏感。对于高于80 K的温度,长时间峰值位移随温度降低而线性增加,但在80 K时,温度在80到30 K之间时,位移平稳并减小。非均匀宽度(500 cm(-1))和重组能量(378 cm(-1))很好地描述了在高温和低温下峰位移的初始值,其衰减,吸收光谱和三脉冲光子回波信号。尽管可以定性地解释动力学对温度的不敏感性,但我们在描述长时间峰位移的温度依赖性方面不是很成功。在低温下,与温度无关的线形函数的虚部对响应有很大贡献,而在高温下,相移主要由线形函数的实部决定。需要一个更复杂的模型来定量描述数据。 (C)1997美国物理研究所。 [参考:58]

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