Engel Robin Y, Ekimova Maria, Miedema Piter S, Kleine Carlo, Ludwig Jan, Ochmann Miguel, Grimm-Lebsanft Benjamin, Ma Rory, Teubner Melissa, Dziarzhytski Siarhei, Brenner Günter, Czwalinna Marie Kristin, Rösner Benedikt, Kim Tae Kyu, David Christian, Herres-Pawlis Sonja, Rübhausen Michael, Nibbering Erik T J, Huse Nils, Beye Martin
Deutsches Elektronen Synchrotron DESY, 22607 Hamburg, Germany.
Max Born Institute for Nonlinear Optics and Short Pulse Spectroscopy, 12489 Berlin, Germany.
Struct Dyn. 2021 Jan 29;8(1):014303. doi: 10.1063/4.0000049. eCollection 2021 Jan.
X-ray absorption near-edge structure (XANES) spectroscopy provides element specificity and is a powerful experimental method to probe local unoccupied electronic structures. In the soft x-ray regime, it is especially well suited for the study of 3-metals and light elements such as nitrogen. Recent developments in vacuum-compatible liquid flat jets have facilitated soft x-ray transmission spectroscopy on molecules in solution, providing information on valence charge distributions of heteroatoms and metal centers. Here, we demonstrate XANES spectroscopy of molecules in solution at the nitrogen -edge, performed at FLASH, the Free-Electron Laser (FEL) in Hamburg. A split-beam referencing scheme optimally characterizes the strong shot-to-shot fluctuations intrinsic to the process of self-amplified spontaneous emission on which most FELs are based. Due to this normalization, a sensitivity of 1% relative transmission change is achieved, limited by fundamental photon shot noise. The effective FEL bandwidth is increased by streaking the electron energy over the FEL pulse train to measure a wider spectral window without changing FEL parameters. We propose modifications to the experimental setup with the potential of improving the instrument sensitivity by two orders of magnitude, thereby exploiting the high peak fluence of FELs to enable unprecedented sensitivity for femtosecond XANES spectroscopy on liquids in the soft x-ray spectral region.
X射线吸收近边结构(XANES)光谱能够提供元素特异性,是探测局部未占据电子结构的一种强大实验方法。在软X射线区域,它特别适合研究3d金属和氮等轻元素。真空兼容液体平面射流的最新进展推动了对溶液中分子的软X射线透射光谱研究,提供了有关杂原子和金属中心价电荷分布的信息。在此,我们展示了在汉堡自由电子激光(FEL)装置FLASH上进行的溶液中分子氮边XANES光谱。一种分束参考方案最佳地表征了大多数FEL所基于的自放大自发辐射过程中固有的强烈逐次脉冲波动。由于这种归一化,实现了1%相对透射率变化的灵敏度,受基本光子散粒噪声限制。通过在FEL脉冲序列上对电子能量进行条纹扫描,有效FEL带宽得以增加,从而在不改变FEL参数的情况下测量更宽的光谱窗口。我们提议对实验装置进行改进,有望将仪器灵敏度提高两个数量级,从而利用FEL的高峰值通量,在软X射线光谱区域实现对液体的飞秒XANES光谱前所未有的灵敏度。