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Rydberg states of small NaArn* clusters

机译:小NaArn *团簇的里德堡州

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The 4s and 5s Rydberg excited states of NaArn* clusters are investigated using a pseudopotential quantum-classical method. While NaArn clusters in their ground state are known to be weakly bound van der Waals complexes with Na lying at the surface of the argon cluster, isomers in 4s or 5s electronically excited states of small NaArn* clusters (n <= 10) are found to be stable versus dissociation. The relationship between electronic excitation and cluster geometry is analyzed as a function of cluster size. For both 4s and 5s states, the stable exciplex isomers essentially appear as sodium-centered structures with similar topologies, converging towards those of the related NaArn+ positive ions when the excitation level is increased. This is consistent with a Rydberg-type picture for the electronically excited cluster, described by a central sodium ion solvated by an argon shell, and an outer diffuse electron orbiting around this NaArn+ cluster core. (c) 2006 American Institute of Physics.
机译:利用伪势量子经典方法研究了NaArn *团簇的4s和5s Rydberg激发态。虽然已知处于基态的NaArn团簇是弱结合的范德华配合物,而Na位于氩团簇的表面,但发现小的NaArn *团簇(n <= 10)处于4s或5s电子激发态的异构体与解离比较稳定。分析电子激发与团簇几何形状之间的关系,作为团簇尺寸的函数。对于4s和5s状态,稳定的激基复合物异构体基本上以具有相似拓扑结构的钠中心结构形式出现,当激发水平提高时,趋向于相关的NaArn +正离子。这与电子激发团簇的Rydberg型照片一致,该图片由氩壳溶解的中心钠离子和围绕该NaArn +团簇核轨道的外部扩散电子描述。 (c)2006年美国物理研究所。

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