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Vibrational dynamics of excited states probed by fs/ps CARS: simulations and applications to ultrafast charge transfer dynamics

机译:fs / ps CARS探测激发态的振动动力学:超快电荷转移动力学的仿真和应用

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摘要

The subpicosecond time evolution of a push-pull stilbene, 4-dimethylamino-4\u27-nitrostilbene (DANS) following 400 nm excitation in acetonitrile is observed with vibrational resolution using the recently-developed fs/ps CARS probe technique. Raman-active modes in the fingerprint region of the vibrational spectrum are observed to evolve, both in intensity and in frequency. The evolution of the DANS vibrational spectrum in the nitro symmetric stretch region is probed, exhibiting a frequency upshift on a 300 fs timescale. These findings agree well with timescales observed in transient absorption/gain experiments and support the formation of an intramolecular charge transfer (ICT) state on a subpicosecond timescale in acetonitrile that precedes the fast (∼12 ps) internal conversion timescale observed in prior studies. Simulations of fs/ps CARS technique help in understanding the experimental transition from time resolved CARS to fs/ps CARS. Simulations indicate an increase in frequency resolution of modes as well as direct measurement of the vibrational modes.
机译:使用最新开发的fs / ps CARS探针以振动分辨率观察到乙腈中400 nm激发后的推挽二苯乙烯,4-二甲基氨基-4 \ u27-硝基苯乙烯(DANS)在亚皮秒时间内的演化。观察到振动光谱的指纹区域中的拉曼活性模式在强度和频率上都在演变。探究了DANS振动光谱在硝基对称拉伸区域中的演化,在300 fs的时间尺度上表现出频率上移。这些发现与瞬态吸收/增益实验中观察到的时间尺度非常吻合,并支持在亚皮秒级的乙腈中形成分子内电荷转移(ICT)状态,该状态早于先前研究中观察到的快速内部转换时间尺度(〜12 ps)。 fs / ps CARS技术的仿真有助于理解从时间分辨的CARS到fs / ps CARS的实验过渡。仿真表明模式频率分辨率的提高以及振动模式的直接测量。

著录项

  • 作者

    Prince, Beth Marie;

  • 作者单位
  • 年度 2008
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  • 原文格式 PDF
  • 正文语种 en
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