arXivDaily arXiv每日学术速递 周一至周五更新
arXiv 1802.04652cond-mat.mtrl-sci
收藏

石墨中的阿秒色散软X射线吸收精细结构谱

Attosecond dispersive soft X-ray absorption fine structure spectroscopy in graphite

Bárbara Buades, Dooshaye Moonshiram, Themistoklis P. H. Sidiropoulos, Iker León, Peter Schmidt, Irina Pi, Nicola Di Palo, Seth L. Cousin, Antonio Picón, Frank Koppens, Jens Biegert

摘要:

固体的相变和分子的结构转变是重要的光诱导过程的典型例子,由于我们不能实时地将电子激发与原子位置相关联,其潜在机制在很大程度上难以理解。在这里,我们提出了一个决定性的一步,这种新的方法的基础上,水窗口覆盖(284 eV至543 eV)阿秒软X射线脉冲,可以同时访问电子和晶格参数,通过色散X射线吸收精细结构(XAFS)光谱。我们验证了attoXAFS与识别的σ* 和π* 轨道的状态密度的贡献,同时在石墨的晶格的四个特征键距。这项工作展示了attoXAFS的概念,作为一个强大的实时调查工具,这是同样适用于气体,液体和凝聚相。

英文摘要:

Phase transitions of solids and structural transformations of molecules are canonical examples of important photo-induced processes, whose underlying mechanisms largely elude our comprehension due to our inability to correlate electronic excitation with atomic position in real time. Here, we present a decisive step towards such new methodology based on water-window-covering (284 eV to 543 eV) attosecond soft X-ray pulses that can simultaneously access electronic and lattice parameters via dispersive X-ray absorption fine-structure (XAFS) spectroscopy. We validate attoXAFS with an identification of the σ* and π* orbital contributions to the density of states in graphite simultaneously with its lattice's four characteristic bonding distances. This work demonstrates the concept of attoXAFS as a powerful real-time investigative tool which is equally applicable to gas-, liquid- and condensed phase.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

↑