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Energy transfer of highly vibrationally excited naphthalene. I. Translational collision energy dependence

机译:高振动激发萘的能量转移。一,平移碰撞能量依赖性

摘要

[[abstract]]Energy transfer between highly vibrationally excited naphthalene and Kr atom in a series of translational collision energies (108–847 cm−1) was studied separately using a crossed-beam apparatus along with time-sliced velocity map ion imaging techniques. Highly vibrationally excited naphthalene in the triplet state (vibrational energy: 16 194 cm−1; electronic energy: 21 400 cm−1) was formed via the rapid intersystem crossing of naphthalene initially excited to the S2 state by 266 nm photons. The collisional energy transfer probability density functions were measured directly from the scattering results of highly vibrationally excited naphthalene. At low collision energies a short-lived naphthalene-Kr complex was observed, resulting in small amounts of translational to vibrational-rotational (TVR) energy transfer. The complex formation probability decreases as the collision energy increases. TVR energy transfer was found to be quite efficient at all collision energies. In some instances, nearly all of the translational energy is transferred to vibrational-rotational energy. On the other hand, only a small fraction of vibrational energy is converted to translational energy. The translational energy gained from vibrational energy extend to large energy transfer (up to 3000 cm−1) as the collision energy increases to 847 cm−1. Substantial amounts of large VT energy transfer were observed in the forward and backward directions at large collision energies.
机译:[[摘要]]使用横梁装置和时间切片速度图离子成像技术分别研究了一系列振动平移碰撞能量(108–847 cm-1)中高振动激发的萘与Kr原子之间的能量转移。三元态的高振动激发萘(振动能:16 194 cm-1;电子能:21 400 cm-1)是通过萘被266 nm光子最初激发到S2状态的快速系统间交叉形成的。碰撞能量转移概率密度函数直接从高度振动激发的萘的散射结果中测量。在低碰撞能量下,观察到寿命短的萘-K络合物,导致少量的平移到振动-旋转(TVR)能量转移。随着碰撞能量的增加,复合物形成概率降低。发现TVR能量转移在所有碰撞能量下都非常有效。在某些情况下,几乎所有的平移能量都转换为振动旋转能量。另一方面,只有一小部分的振动能转化为平移能。当碰撞能量增加到847 cm-1时,从振动能量获得的平移能量会扩展到较大的能量传递(最大3000 cm-1)。在大的碰撞能量下,在向前和向后的方向上观察到大量的大的VT能量转移。

著录项

  • 作者

    Chen-Lin Liu;

  • 作者单位
  • 年度 2011
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  • 原文格式 PDF
  • 正文语种 [[iso]]en
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