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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Ultrafast Dynamics at the Na/D2O/Cu(111) Interface: Electron Solvation in Ice Layers and Na~+-Mediated Surface Solvation
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Ultrafast Dynamics at the Na/D2O/Cu(111) Interface: Electron Solvation in Ice Layers and Na~+-Mediated Surface Solvation

机译:Na / D2O / Cu(111)界面上的超快动力学:冰层中的电子溶剂化和Na〜+介导的表面溶剂化

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摘要

We have studied the influence of sodium ions bound near the ice/vacuum interface on the electron solvation dynamics in amorphous D2O ice layers by means of femtosecond time-resolved two-photon photoelectron spectroscopy. Adsorption of submonolayer coverages of sodium on top of multilayers of amorphous ice leads to the formation of Na~+ ions and to pronounced changes in the observed ultrafast dynamics compared to pure amorphous ice. We identify a Na~+-induced species of excess electrons which exhibits a much longer lifetime compared to excess electrons in pure D2O ice and approximate the decay of the Na-induced contribution by two decay times τ2 = 880 fs and τ3 = 9.6 ps. In addition, a faster energetic stabilization of the excited electrons with a rate of Σ = 0.73 eV/ps is observed. The population of these electrons depends nonlinearly on the sodium coverage. We attribute the Na-induced contribution to a transient electron/ion/water complex which is located at the ice/vacuum interface. This interpretation is corroborated by coverage-dependent measurements and by overlayer experiments.
机译:我们已经通过飞秒时间分辨双光子光电子能谱研究了结合在冰/真空界面附近的钠离子对非晶D2O冰层中电子溶剂化动力学的影响。与无定形冰的多层相比,亚单层覆盖的钠吸附在无定形冰的多层上导致形成Na〜+离子,并导致观察到的超快动力学发生明显变化。我们确定了Na〜+诱导的过量电子种类,与纯D2O冰中的过量电子相比,它们具有更长的寿命,并通过两个衰减时间τ2= 880 fs和τ3= 9.6 ps近似估算Na诱导的贡献的衰减。另外,观察到被激发的电子具有Σ= 0.73 eV / ps的更快的能量稳定。这些电子的数量非线性地取决于钠的覆盖率。我们将钠诱导的贡献归因于位于冰/真空界面的瞬态电子/离子/水复合物。这种解释被覆盖率相关的测量和覆盖层实验所证实。

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