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Stimulated X-Ray Emission Spectroscopy in Transition Metal Complexes

机译:过渡金属配合物中的受激X射线发射光谱

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摘要

We report the observation and analysis of the gain curve of amplified Kα x-ray emission from solutions of Mn(II) and Mn(VII) complexes using an x-ray free electron laser to create the 1s core-hole population inversion. We find spectra at amplification levels extending over 4 orders of magnitude until saturation. We observe bandwidths below the Mn 1s core-hole lifetime broadening in the onset of the stimulated emission. In the exponential amplification regime the resolution corrected spectral width of ~1.7 eV FWHM is constant over 3 orders of magnitude, pointing to the buildup of transform limited pulses of ~1 fs duration. Driving the amplification into saturation leads to broadening and a shift of the line. Importantly, the chemical sensitivity of the stimulated x-ray emission to the Mn oxidation state is preserved at power densities of ~1020 W/cm2 for the incoming x-ray pulses. Differences in signal sensitivity and spectral information compared to conventional (spontaneous) x-ray emission spectroscopy are discussed. Our findings build a baseline for nonlinear x-ray spectroscopy for a wide range of transition metal complexes in inorganic chemistry, catalysis, and materials science.
机译:我们报告观察和分析使用X射线自由电子激光从Mn(II)和Mn(VII)配合物溶液中放大的KαX射线发射的增益曲线,以创建1s核心孔人口反演。我们发现放大水平上的光谱扩展了4个数量级,直到达到饱和为止。我们观察到,在受激发射的开始时,Mn 1s核孔寿命以下的带宽变宽。在指数放大方案中,〜1.7 eV FWHM的分辨率校正光谱宽度在3个数量级上是恒定的,这表明持续时间约为1 fs的变换受限脉冲的建立。驱动放大到饱和导致线变宽和偏移。重要的是,对于入射的X射线,功率密度为〜10 20 W / cm 2 时,可以保持激发的X射线发射对Mn氧化态的化学敏感性。脉冲。讨论了与常规(自发)X射线光谱相比信号灵敏度和光谱信息的差异。我们的发现为无机化学,催化和材料科学中的多种过渡金属配合物建立了非线性X射线光谱的基线。

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