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Polarization effects on electronic excitation of molecules by low-energy electron impact: Study one−-furan scattering

机译:低能量电子影响对分子电子激发的极化效应:研究一 - 呋喃散射

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摘要

The Schwinger multichannel method is applied to study the influence of polarization effects on the electronic excitation of the furan molecule by low-energy electron impact. We discuss the importance of inclusion of these effects through the comparison of theoretical results for the electronic excitation of the B3 2 state of furan obtained with and without the proper treatment of the polarization of the target. The electron-furan scattering presents two prominent shape resonances in the A2 2 and B2 1 symmetries at around the electronic excitation threshold of the B3 2 state (3.7 eV). At this low-energy, the inclusion of polarization effects in the calculation moves to lower energies the resonances positions obtained either in the close-coupling or in the static-exchange level of approximation. This phenomenon strongly influences the electronic excitation process. The present results show that a simple close-coupling calculation cannot be applied for molecular systems with low-energy electronic excitation thresholds around misplaced resonances. © 2008 The American Physical Society.
机译:应用施威格多氏多通道方法研究极化效应对呋喃分子的电子激发对低能量电子的影响。我们讨论了通过对呋喃的电子激发的理论结果的比较来讨论包含这些效果的重要性,并且没有适当治疗靶标的极化的正确处理。电子散射呋喃呈现两个突出的形状的共振在A2 2和B2 1对称性在围绕B3 2状态(3.7电子伏特)的电子激励的阈值。在该低能量下,在计算中包含偏振效应移动以降低能量在近耦合或静态交换水平中获得的谐振位置。这种现象强烈影响电子励磁过程。本结果表明,在错位的共振周围具有低能量电子激发阈值的分子系统,不能施加简单的紧密耦合计算。 ©2008美国的物理社会。

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