Wrede Eckart, Schnieder Ludger, Seekamp-Schnieder Karen, Niederjohann Britta, Welge Karl H
Faculty of Physics, University of Bielefeld, 33615 Bielefeld, Germany.
Phys Chem Chem Phys. 2005 Apr 7;7(7):1577-82. doi: 10.1039/b417440b.
The scattering of highly excited hydrogen Rydberg atoms, H* (n = 36), with deuterium molecules in their rovibrational ground state, D2(v = 0, j = 0), has been investigated at a relative collision energy of 0.53 eV. Time-of-flight distributions of elastically/inelastically scattered H* Rydberg atoms and reactively scattered D* Rydberg atoms have been measured at different laboratory angles. The extracted rovibrationally resolved state distributions of the HD product molecules from reactive collisions resemble closely those reported for the corresponding ion-molecule reaction, H+ + D2 --> HD + D+. This similarity is rationalised using the free electron model which predicts that the Rydberg electron acts as a spectator while the ionic reaction takes place.
在相对碰撞能量为0.53电子伏特的条件下,对处于高激发态的氢里德堡原子H*(n = 36)与处于振转基态的氘分子D2(v = 0,j = 0)的散射进行了研究。在不同的实验室角度测量了弹性/非弹性散射的H里德堡原子以及反应性散射的D里德堡原子的飞行时间分布。从反应性碰撞中提取的HD产物分子的振转分辨态分布与相应的离子 - 分子反应H+ + D2 → HD + D+所报道的分布非常相似。利用自由电子模型对这种相似性进行了合理化解释,该模型预测在离子反应发生时,里德堡电子起旁观者的作用。