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Joint Analysis of Radiative and Non-Radiative Electronic Relaxation Upon X-ray Irradiation of Transition Metal Aqueous Solutions

机译:过渡金属水溶液在X射线辐照下的辐射和非辐射电子弛豫的联合分析

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摘要

L-edge soft X-ray spectroscopy has been proven to be a powerful tool to unravel the peculiarities of electronic structure of transition metal compounds in solution. However, the X-ray absorption spectrum is often probed in the total or partial fluorescence yield modes, what leads to inherent distortions with respect to the true transmission spectrum. In the present work, we combine photon- and electron-yield experimental techniques with multi-reference first principles calculations. Exemplified for the prototypical FeCl2 aqueous solution we demonstrate that the partial yield arising from the Fe3s → 2p relaxation is a more reliable probe of the absorption spectrum than the Fe3d → 2p one. For the bonding-relevant 3d → 2p channel we further provide the basis for the joint analysis of resonant photoelectron and inelastic X-ray scattering spectra. Establishing the common energy reference allows to assign both spectra using the complementary information provided through electron-out and photon-out events.
机译:L边缘软X射线光谱法已被证明是揭示溶液中过渡金属化合物电子结构特性的有力工具。然而,经常在全部或部分荧光产生模式中探测X射线吸收光谱,这导致相对于真实透射光谱的固有失真。在目前的工作中,我们将光子和电子屈服实验技术与多参考第一原理计算相结合。以典型的FeCl2水溶液为例,我们证明了Fe3s→2p弛豫所产生的部分收率是比Fe3d→2p吸收光谱更可靠的探针。对于与键相关的3d→2p通道,我们进一步为共振光电子和非弹性X射线散射光谱的联合分析提供了基础。建立公共能量参考可以使用通过电子输出和光子输出事件提供的补充信息来分配两个光谱。

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