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Genuine binding energy of the hydrated electron

机译:水合电子的真正结合能

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The unknown influence of inelastic and elastic scattering of slow electrons in water has made it difficult to clarify the role of the solvated electron in radiation chemistry and biology. We combine accurate scattering simulations with experimental photoemission spectroscopy of the hydrated electron in a liquid water microjet, with the aim of resolving ambiguities regarding the influence of electron scattering on binding energy spectra, photoelectron angular distributions, and probing depths. The scattering parameters used in the simulations are retrieved from independent photoemission experiments of water droplets. For the ground-state hydrated electron, we report genuine values devoid of scattering contributions for the vertical binding energy and the anisotropy parameter of 3.7 ± 0.1 eV and 0.6 ± 0.2, respectively. Our probing depths suggest that even vacuum ultraviolet probing is not particularly surface-selective. Our work demonstrates the importance of quantitative scattering simulations for a detailed analysis of key properties of the hydrated electron.
机译:水中慢速电子的非弹性和弹性散射的未知影响使得难以阐明溶剂化电子在辐射化学和生物学中的作用。我们将精确的散射模拟与液态水微射流中水合电子的实验性光发射光谱学结合起来,以解决关于电子散射对结合能谱,光电子角分布和探测深度的影响的歧义。模拟中使用的散射参数是从独立的水滴光发射实验中获得的。对于基态水合电子,我们报告的真实值不含垂直键合能和各向异性参数分别为3.7±0.1 eV和0.6±0.2的散射贡献。我们的探测深度表明,即使是真空紫外线探测也没有特别的表面选择性。我们的工作证明了定量散射模拟对于详细分析水合电子关键特性的重要性。

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