Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai 980-8577, Japan.
J Chem Phys. 2013 Sep 28;139(12):124306. doi: 10.1063/1.4820814.
We report unambiguous experimental and theoretical evidence of intramolecular photoelectron diffraction in the collective vibrational excitation that accompanies high-energy photoionization of gas-phase CF4, BF3, and CH4 from the 1s orbital of the central atom. We show that the ratios between vibrationally resolved photoionization cross sections (v-ratios) exhibit pronounced oscillations as a function of photon energy, which is the fingerprint of electron diffraction by the surrounding atomic centers. This interpretation is supported by the excellent agreement between first-principles static-exchange and time-dependent density functional theory calculations and high resolution measurements, as well as by qualitative agreement at high energies with a model in which atomic displacements are treated to first order of perturbation theory. The latter model allows us to rationalize the results for all the v-ratios in terms of a generalized v-ratio, which contains information on the structure of the above three molecules and the corresponding molecular cations. A fit of the measured v-ratios to a simple formula based on this model suggests that the method could be used to obtain structural information of both neutral and ionic molecular species.
我们报告了明确的实验和理论证据,证明在气相 CF4、BF3 和 CH4 的中心原子 1s 轨道高能光致电离伴随的集体振动激发中存在分子内光电离衍射。我们表明,振动分辨光致电离截面比(v-比)与光子能量的函数关系呈现出明显的振荡,这是电子通过周围原子中心衍射的特征。这种解释得到了第一性原理静态交换和含时密度泛函理论计算以及高分辨率测量之间极好一致性的支持,并且在高能下与一个将原子位移一阶微扰理论处理的模型定性一致。后一个模型使我们能够根据一个包含上述三种分子和相应的分子阳离子结构信息的广义 v-比来合理化所有 v-比的结果。通过将测量的 v-比拟合到基于该模型的简单公式,表明该方法可用于获得中性和离子分子物种的结构信息。