Grabau Mathias, Erhard Jannis, Taccardi Nicola, Calderon Sandra Krick, Wasserscheid Peter, Görling Andreas, Steinrück Hans-Peter, Papp Christian
Lehrstuhl für Physikalische Chemie II, Friedrich-Alexander Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058, Erlangen, Germany.
Lehrstuhl für Theoretische Chemie, Friedrich-Alexander Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058, Erlangen, Germany.
Chemistry. 2017 Dec 14;23(70):17701-17706. doi: 10.1002/chem.201703627. Epub 2017 Nov 6.
Liquid binary Pd-Ga alloys with low Pd contents of 0.8, 1.8, and 4.7 at % of Pd were examined as a function of sample temperature in ultra-high vacuum by using angle-resolved XPS. Upon cooling from 750 to 400 K, a pronounced temperature-dependence of the Pd concentration in the liquid phase was observed, which was explained by the transition from the pure liquid phase to a two-phase system, consisting of a solid Ga Pd phase and a Pd-depleted liquid Pd-Ga alloy. In the liquid Pd-Ga alloy, Pd is always depleted from the topmost interface layer, as deduced from angle-resolved XPS at 0 and 80° emission, independent of temperature and Pd concentration. This observation is interpreted as an inhomogeneous depth distribution function of Pd, that is, the segregation of Ga to the surface of the liquid phase. The results of a DFT-based molecular dynamics simulation (MD) independently show interfacial stratification of Ga and an inhomogeneous Pd distribution along the surface normal. The evaluation of the experimental data with a rigid layer model based on the MD calculations leads to excellent agreement with the simulation.
通过角分辨X射线光电子能谱(angle-resolved XPS),在超高真空条件下,研究了钯(Pd)含量分别为0.8、1.8和4.7原子百分比的液态二元Pd-Ga合金随样品温度的变化情况。从750K冷却至400K时,观察到液相中Pd浓度呈现出明显的温度依赖性,这是由于从纯液相转变为包含固态Ga Pd相和贫Pd液态Pd-Ga合金的两相体系所致。在液态Pd-Ga合金中,根据0°和80°发射角的角分辨XPS推断,Pd总是从最顶层界面层贫化,且与温度和Pd浓度无关。这一观察结果被解释为Pd的非均匀深度分布函数,即Ga在液相表面的偏析。基于密度泛函理论(DFT)的分子动力学模拟(MD)结果独立显示了Ga的界面分层以及沿表面法线方向的Pd非均匀分布。基于MD计算的刚性层模型对实验数据的评估与模拟结果高度吻合。