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氩团簇上钾原子的光谱学与动力学

Spectroscopy and Dynamics of K Atoms on Argon Clusters.

作者信息

Douady J, Awali S, Poisson L, Soep B, Mestdagh J M, Gervais B

机构信息

†Unité mixte CEA-CNRS-ENSICAEN-UCBN 6252 BP 5133, CIMAP, F-14070 Caen, Cedex 05, France.

‡Laboratoire Francis Perrin, URA 2453, CEA/IRAMIS/LIDYL, F-91191 Gif-sur-Yvette, France.

出版信息

J Phys Chem A. 2015 Jun 11;119(23):6074-81. doi: 10.1021/jp512691s. Epub 2015 Apr 21.

DOI:10.1021/jp512691s
PMID:25854161
Abstract

We present a combined experimental and simulation study of the 4s → 4p photoexcitation of the K atom trapped at the surface of ArN clusters made of a few hundred Ar atoms. Our experimental method based on photoelectron spectroscopy allows us to firmly establish that one single K atom is trapped at the surface of the cluster. The absorption spectrum is characterized by the splitting of the atomic absorption line into two broad bands, a Π band associated with p orbitals parallel to the cluster surface and a Σ band associated with the perpendicular orientation. The spectrum is consistent with observations reported for K atoms trapped on lighter inert gas clusters, but the splitting between the Π and Σ bands is significantly larger. We show that a large amount of K atoms are transiently stuck and eventually lost by the Ar cluster, in contrast with previous observations reported for alkaline earth metal systems. The excitation in the Σ band leads systematically to the ejection of the K atom from the Ar cluster. On the contrary, excitation in the Π band leads to the formation of a bound state. In this case, the analysis of the experimental photoelectron spectrum by means of nonadiabatic molecular dynamics simulation shows that the relaxation drives the system toward a basin where the coordination of the K atom is 2.2 Ar atoms on the average, in a poorly structured surface.

摘要

我们展示了一项针对被困在由几百个氩原子构成的ArN团簇表面的钾原子4s→4p光激发的实验与模拟相结合的研究。我们基于光电子能谱的实验方法使我们能够确定有单个钾原子被困在团簇表面。吸收光谱的特征是原子吸收线分裂为两个宽带,一个与平行于团簇表面的p轨道相关的Π带,以及一个与垂直取向相关的Σ带。该光谱与报道的被困在较轻惰性气体团簇上的钾原子的观测结果一致,但Π带和Σ带之间的分裂明显更大。我们表明,与先前报道的碱土金属系统的观测结果相反,大量钾原子会短暂附着在氩团簇上并最终从团簇上损失。Σ带中的激发会系统地导致钾原子从氩团簇中弹出。相反,Π带中的激发会导致形成束缚态。在这种情况下,通过非绝热分子动力学模拟对实验光电子能谱进行分析表明,弛豫将系统驱动到一个盆地,在这个结构较差的表面上,钾原子的平均配位为2.2个氩原子。

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