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Photoelectron Diffraction Imaging of a Molecular Breakup Using an X-Ray Free-Electron Laser

机译:使用X射线自由电子激光器的分子分解的光电子衍射成像

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A central motivation for the development of x-ray free-electron lasers has been the prospect of timeresolved single-molecule imaging with atomic resolution. Here, we show that x-ray photoelectron diffraction—where a photoelectron emitted after x-ray absorption illuminates the molecular structure from within—can be used to image the increase of the internuclear distance during the x-ray-induced fragmentation of an O2 molecule. By measuring the molecular-frame photoelectron emission patterns for a two-photon sequential K-shell ionization in coincidence with the fragment ions, and by sorting the data as a function of the measured kinetic energy release, we can resolve the elongation of the molecular bond by approximately 1.2 a.u. within the duration of the x-ray pulse. The experiment paves the road toward timeresolved pump-probe photoelectron diffraction imaging at high-repetition-rate x-ray free-electron lasers.
机译:X射线自由电子激光器的开发的中心动机一直是具有原子分辨率的Timeresolved单分子成像的前景。在这里,我们表明X射线光电子电子衍射 - 其中发出的光电子在X射线吸收之后照射来自内部的分子结构 - 可用于图像在X射线诱导的O2分子的碎片中的间隙距离增加。通过测量与片段离子重合的双光子顺序k-壳电离的分子框架光电子发射图案,并通过将数据作为测量的动能释放的函数进行分类,我们可以解决分子键的伸长率大约1.2 au在X射线脉冲的持续时间内。该实验在高重复率X射线自由电子激光器下朝向Timeresolved泵浦探针光电子电子元件衍射成像的道路。
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