Ding Thomas, Rebholz Marc, Aufleger Lennart, Hartmann Maximilian, Stooß Veit, Magunia Alexander, Birk Paul, Borisova Gergana Dimitrova, da Costa Castanheira Carina, Rupprecht Patrick, Mi Yonghao, Gaumnitz Thomas, Loh Zhi-Heng, Roling Sebastian, Butz Marco, Zacharias Helmut, Düsterer Stefan, Treusch Rolf, Ott Christian, Pfeifer Thomas
Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany.
Laboratorium für Physikalische Chemie, ETH Zürich, Vladimir-Prelog-Weg 2, 8093 Zürich, Switzerland.
Faraday Discuss. 2021 May 27;228(0):519-536. doi: 10.1039/d0fd00107d.
The emergence of ultra-intense extreme-ultraviolet (XUV) and X-ray free-electron lasers (FELs) has opened the door for the experimental realization of non-linear XUV and X-ray spectroscopy techniques. Here we demonstrate an experimental setup for an all-XUV transient absorption spectroscopy method for gas-phase targets at the FEL. The setup combines a high spectral resolving power of E/ΔE ≈ 1500 with sub-femtosecond interferometric resolution, and covers a broad XUV photon-energy range between approximately 20 and 110 eV. We demonstrate the feasibility of this setup firstly on a neon target. Here, we intensity- and time-resolve key aspects of non-linear XUV-FEL light-matter interactions, namely the non-resonant ionization dynamics and resonant coupling dynamics of bound states, including XUV-induced Stark shifts of energy levels. Secondly, we show that this setup is capable of tracking the XUV-initiated dissociation dynamics of small molecular targets (oxygen and diiodomethane) with site-specific resolution, by measuring the XUV transient absorption spectrum. In general, benefitting from a single-shot detection capability, we show that the setup and method provides single-shot phase-locked XUV pulse pairs. This lays the foundation to perform, in the future, experiments as a function of the XUV interferometric time delay and the relative phase, which enables advanced coherent non-linear spectroscopy schemes in the XUV and X-ray spectral range.
超强极紫外(XUV)和X射线自由电子激光(FEL)的出现为非线性XUV和X射线光谱技术的实验实现打开了大门。在此,我们展示了一种用于FEL气相靶标的全XUV瞬态吸收光谱法的实验装置。该装置将E/ΔE≈1500的高光谱分辨率与亚飞秒干涉分辨率相结合,覆盖了约20至110 eV的宽XUV光子能量范围。我们首先在氖靶上证明了该装置的可行性。在此,我们对非线性XUV-FEL光与物质相互作用的关键方面进行强度和时间分辨,即束缚态的非共振电离动力学和共振耦合动力学,包括XUV诱导的能级斯塔克位移。其次,我们表明该装置能够通过测量XUV瞬态吸收光谱,以位点特异性分辨率跟踪小分子靶标(氧气和二碘甲烷)的XUV引发的解离动力学。一般来说,受益于单次检测能力,我们表明该装置和方法提供单次锁相XUV脉冲对。这为未来根据XUV干涉时间延迟和相对相位进行实验奠定了基础,从而能够在XUV和X射线光谱范围内实现先进的相干非线性光谱方案。