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ANGLE-SCANNED PHOTOELECTRON DIFFRACTION: A STRUCTURAL PROBE FOR NEAR-SURFACE ATOMIC LAYERS

机译:角度倾斜的光电子衍射:近表面原子层的结构探针

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摘要

Electrons emitted from the core levels of a photon-irradiated crystalline sample undergo scattering by atoms in the vicinity of the emitting species. Subsequent interference phenomena between the electron wave portions propagating to the detector produce intensity modulations as a function of the direction of detection. This process constitutes the physical basis of the angle-scanned X-ray Photoelectron Diffraction (XPD) technique. The resulting modulations, properly interpreted, are rich in structural information concerning the near-surface atomic layers. In the present notes, after an introduction to the principles of XPD, some selected results in the field of chemisorption and ultrathin epitaxial films will be reported in order to outline the merits of the technique. Qualitative structural information (e.g. growth modes and lattice distortions, orientation of chemisorbed molecules) can be directly obtained from the experimental raw data without any need of theoretical simulation. On the other hand, quantitative structural parameters and chemisorption sites may be deduced by using a trial-and-error fitting procedure based on simple single-scattering models.
机译:从受光子照射的晶体样品的核能级发射的电子受到发射物质附近原子的散射。传播到检测器的电子波部分之间的随后干涉现象产生强度调制,该强度调制是检测方向的函数。此过程构成了角度扫描X射线光电子衍射(XPD)技术的物理基础。经过适当解释后,得到的调制富含有关近表面原子层的结构信息。在本说明中,在介绍XPD原理之后,将报告化学吸附和超薄外延膜领域的一些选定结果,以概述该技术的优点。定性结构信息(例如生长模式和晶格畸变,化学吸附分子的取向)可以直接从实验原始数据中获得,而无需理论模拟。另一方面,可以通过基于简单的单散射模型的试错拟合程序来推导定量的结构参数和化学吸附位点。

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