Ultrafast charge redistribution in small iodine containing molecules

被引:7
|
作者
Hollstein, M. [1 ]
Mertens, K. [2 ]
Klumpp, S. [3 ]
Gerken, N. [2 ]
Palutke, S. [3 ]
Baev, I [2 ]
Brenner, G. [3 ]
Dziarzhytski, S. [3 ]
Meyer, M. [4 ]
Wurth, W. [2 ,3 ]
Pfannkuche, D. [1 ]
Martins, M. [2 ]
机构
[1] Univ Hamburg, Dept Phys, Jungiusstr 9, D-20355 Hamburg, Germany
[2] Univ Hamburg, Dept Phys, Luruper Chaussee 149, D-22761 Hamburg, Germany
[3] DESY, Notkestr 85, D-22607 Hamburg, Germany
[4] European XFEL GmbH, Holzkoppel 4, D-22869 Schenefeld, Germany
来源
NEW JOURNAL OF PHYSICS | 2019年 / 21卷
基金
欧盟地平线“2020”;
关键词
photoionization; free electron laser; xuv pump- xuv probe; charge rearrangement; FREE-ELECTRON LASER; MONOCHROMATOR BEAMLINE; POPULATION ANALYSIS; CROSS-SECTIONS; RAY; FRAGMENTATION; PERFORMANCE; DYNAMICS;
D O I
10.1088/1367-2630/ab1056
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We present studies on intra-molecular charge redistribution in iodine containing molecules upon iodine-4d photoionization. For this, we employed an XUV-pump-XUV-probe scheme based on time-delayed femtosecond pulses delivered by the free-electron laser at DESY in Hamburg (FLASH). The experimental results show delay dependent and molecule-specific iodine charge state distributions that arise upon multiple iodine-4d photoionization. Using the example of CH3I and CH2I2, we compare the delay-dependent yields of I3+. We model the involved processes using advanced ab initio electronic structure calculations which include electron correlations combined with a classical model of the nuclear motion. The qualitative agreement of our model with the experimental results allows us to relate the observed, strongly molecule-specific efficiencies of the intra-molecular charge rearrangement not only to molecule-specific fragmentation timescales but also to molecule-specific electronic structure and molecular environment.
引用
收藏
页数:9
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