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首页> 外文期刊>The European Physical Journal B >Time-resolved Fourier-transform infrared reflection study on photoinduced phase transition of tetrathiafulvalene-p-chloranil crystal
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Time-resolved Fourier-transform infrared reflection study on photoinduced phase transition of tetrathiafulvalene-p-chloranil crystal

机译:时间分辨傅立叶变换红外反射研究四硫富瓦烯-对氯苯醌晶体的光诱导相变

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摘要

We have measured temporal change of infrared reflection spectrum of ionic phase of tetrathiafulvalene-p-chloranil (TTF-CA) crystal induced by 10 ns pulsed laser excitation at 2.35 eV with using a step-scan Fourier-transform infrared spectrometer. The excitation reduced the magnitude of the a g -mode bands around 980 cm-1 and 1380 cm-1 and enhanced reflection intensity at 1630 cm-1. The time evolution of both the a g -mode changes and the enhancement at 1630 cm-1 are described by the sum of two decay components: one decayed within 2 μs and the other showed very gradual decay within the time range used in the present study. The fractional changes of reflectivity for the fast decay components were almost identical for all a g modes. The 1630 cm-1 enhancement can be ascribed to the carbonyl stretching vibration of CA. The position of this peak shifts slightly to low-wavenumber side from the CA peak of the neutral phase in thermal equilibrium. Consequently, the fast decay component is ascribed to the photoinduced phase. The slow decay component is conceivably due to the metastable center formed by the excitation, because we could not resolve the spectral change corresponding to the slow component in the range between 1595 and 1660 cm-1, where the carbonyl stretching vibration of TTF-CA is observed. The degree of charge transfer of the photoinduced phase is evaluated to 0.52 ± 0.08 by comparing the peak position of the transient enhancement with those of the carbonyl stretching vibration modes in ionic and neutral phases in thermal equilibrium.
机译:我们使用步进扫描傅立叶变换红外光谱仪测量了在2.35 eV处10 ns脉冲激光激发引起的四硫富瓦烯-对氯甲腈(TTF-CA)离子相的红外反射光谱的时间变化。激发降低了980 cm-1和1380 cm-1附近的a g型谱带的强度,并增强了1630 cm-1处的反射强度。 a g模式变化和1630 cm-1处增强的时间演化由两个衰减分量之和描述:一个衰减在2μs之内,另一个衰减在本研究使用的时间范围内逐渐衰减。对于所有g模式,快速衰减分量的反射率的分数变化几乎相同。 1630 cm-1的增强可归因于CA的羰基拉伸振动。在热平衡中,该峰的位置从中性相的CA峰稍微移至低波数侧。因此,快速衰减分量归因于光诱导相。缓慢衰减的成分可能是由于激发形成的亚稳态中心,因为我们无法解析对应于1595和1660 cm-1之间的缓慢成分的光谱变化,其中TTF-CA的羰基拉伸振动为观测到的。通过在离子和中性相的热平衡状态下比较瞬态增强峰和羰基拉伸振动模态的峰值位置,将光诱导相的电荷转移程度评估为0.52±0.08。

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  • 来源
    《The European Physical Journal B》 |2013年第3期|1-6|共6页
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    Department of Materials Science and Chemistry Wakayama University">(1109);

    Department of Materials Science and Chemistry Wakayama University">(1109);

    Department of Materials Science and Chemistry Wakayama University">(1109);

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