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Low-energy electron scattering from C3H4 isomers: Differential cross sections for elastic scattering and vibrational excitation - art. no. 032714

机译:来自C3H4异构体的低能电子散射:用于弹性散射和振动激发的微分截面-艺术。没有。 032714

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摘要

Absolute differential cross sections (DCSs) for elastic and vibrationally inelastic scattering of electrons from C3H4 isomers (allene and propyne) have been determined by a crossed-beam experiment in the energy range 1.5-100 eV and over the scattering angles between 15degrees-130degrees. The relative flow method was applied to normalize these cross sections, using helium as a standard. Clear evidence of the strong isomer effect has been observed in DCSs for both elastic and vibrational excitation processes, and the isomer effect still conspicuously persists in total elastic cross sections. Two resonance regions where the vibrational cross sections are strongly enhanced are observed in both allene and propyne below a few eV, while both the DCSs become identical at higher energies, hence weakening the isomer effect. More details of the observed mode selectivity are discussed based on the selection rules for vibrational excitation via a shape resonance as well as on an argument based on the angular correlation. [References: 29]
机译:已经通过交叉电子束实验在能量范围1.5-100 eV以及在15度-130度之间的散射角上确定了来自C3H4异构体(丙二烯和丙炔)的电子发生弹性和振动非弹性散射的绝对微分截面(DCS)。以氦为标准,采用相对流动法将这些截面归一化。在DCS中,在弹性和振动激发过程中都观察到了强大的异构体效应的清晰证据,并且该异构体效应仍然明显地存在于整个弹性截面中。在低于几个eV的丙二烯和丙炔中均观察到两个振动区域,振动截面都大大增强,而两个DCS在较高能量下变得相同,因此削弱了异构体效应。基于通过形状共振的振动激励的选择规则以及基于角度相关性的自变量,讨论了观测模式选择性的更多细节。 [参考:29]

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