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Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction

机译:成像ar + + H2电荷中的状态到状态反应散射   转移反应

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摘要

The charge transfer reaction of Ar+ with H2 and D2 has been investigated inan experiment combining crossed beams with three-dimensional velocity mapimaging. Angle-differential cross sections for two collision energies have beenobtained for both neutral species. We find that the product ions are highlyinternally excited. In the reaction with H2 the spin-orbit excited Ar+ state'scoupling to the 'resonant' vibrationally excited product H2+(v=2) dominates forboth investigated energies, in line with previous investigations. The observedangular distributions, however, show significantly less back-scattering thanwas found previously. Furthermore, we discovered that the product ions arehighly rotationally excited. In the case of Ar+ reacting with D2 theenergetically closest lying vibrational levels are not strictly preferred andhigher-lying vibrational levels are also populated. For both species thebackward-scattered products show higher internal excitation.
机译:在结合交叉束与三维速度映射成像的实验中,研究了Ar +与H2和D2的电荷转移反应。对于这两种中性物质,已经获得了两种碰撞能量的角度差截面。我们发现产物离子是高度内部激发的。与以前的研究一致,在与H2的反应中,自旋轨道激发的Ar +状态“聚集”到“共振”振动激发产物H2 +(v = 2)占主导地位。然而,观察到的角分布显示出比以前发现的明显少的反向散射。此外,我们发现产物离子是高度旋转激发的。在Ar +与D2反应的情况下,严格地讲,从能量上讲,最不靠近的振动水平不是严格优选的,并且较高的振动水平也被填充。对于这两个物种,向后散射的产品均显示出较高的内部激发。

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